a drug marketed under its chemical name, instead of a brand name

A drug produced and marketed under its chemical or "generic" name (e.g. acetaminophen) as opposed to "Tylenol", a brand name for the former produced by Johnson & Johnson. A generic drug can be sold only after a proprietary drug goes off patent (i.e. when the patent runs out after 17 years). There are numerous generic drug manufacturers. While generic drugs are cheaper for consumers, they still must meet the standards of GMPs as set out by the FDA.

a pharmacological agent approved by the FDA as a bioequivalent substitute and manufactured by a number of different companies as a result of the expiration of the original patent.

drug product that is no longer protected by a commercial patent, meaning any manufacturer has the rights to produce and sell it, as cheaply as possible. After a drug's patent has expired, generic versions of the same compound will be rushed on to the market to compete with the original branded version. Health plans often treat branded and generic drugs as if they were exactly the same drug - even though they are often made in different ways, often using different sources of ingredients.

a Prescription Drug approved by the FDA as a bioequivalent substitute and manufactured by one or more companies as a result of the expiration of the original patent for the equivalent Brand Name Drug. Brand Name Drugs that are crosslicensed to other companies, who then market the brand name drug under a Generic name prior to the patent expiring may be considered and processed under the Brand name level of benefits.

Drug product sold under a branded drug's chemical name, following the expiration of the pertinent patents to the branded drug. Drug patents are issued for 20 years from time of filing. The active ingredients in the branded and generic products are the same. Both the branded and the generic versions must have the same potency, be available in the same dosage forms (i.e. tablet, liquid, injectable), be demonstrated safe and effective, and be manufactured under government-approved GMPs.

Prescription medicines equal in therapeutic effect to brand-name originals, which contain identical active ingredients at the same doses.

prescription medications that are produced by multiple manufacturers and not identified by a brand name.

A pharmaceutical product which is not protected by a patent in force, and which is commercialized under a non-proprietary name or a brand name.

A drug product that is no longer covered by patent protection and thus may be produced and/or distributed by many firms.

The chemical or generic name, as determined by the United States Adopted Names Council (USANC) and accepted by the Federal Food and Drug Administration (FDA), of those drug products having the same active ingredients as prescribed brand name drugs.

A copy of a brand name drug that no longer is protected by a patent. Generic drugs are therapeutically equivalent to the original and are less expensive.

A drug marketed under its biochemical name rather than under a trade brand name. A generic drug differs from its brand-name counterpart in the composition of its inert components, and is typically less expensive than its brand-name equivalent.

A drug that is therapeutically equivalent (identical in strength, concentration, and dosage form) to a brand-name drug and that generally is made available when patent protection expires on the brand-name drug. The term is commonly used to identify a non-brand drug that is sold at a lower cost and generally requires a lower co-payment amount by the member selecting the generic drug.

a drug that has the same chemical ingredients of an advertised brand name drug. The Plan provides greater benefits when you choose a generic drug over a brand name drug when filling a prescription.

when the patent protection for a brand-name drug expires generic versions of the drug can be offered for sale if the FDA agrees; "generic drugs are usually cheaper than brand-name drugs"

a chemical copy of the brand name drug

a chemically equivalent, lower - cost version of a brand - name drug

a copy of a drug of the mark that has expired patent

a copy of an original, pioneer drug product

a copy of a patented medicine that is no longer protected by trademark

a copy of its branded version in terms of dosage, quality, safety, strength and performance

a copy of the brand-name drug with the same dosage, safety, strength, quality, how it is taken, performance, and intended use

a copy of the original drug that is no longer protected by a US patent

a copy that is identical to a brand-name drug in dosage, safety, strength, how it is taken, quality, performance and intended use

a copy that is the same as a brand-name drug in dosage,

a drug based on a branded product but made by a different manufacturer

a drug product that is equivalent to brand name products in terms of quality and performance

a drug which is identical or equivalent to a brand name drug in dosage

a duplicate of a brand name drug

a former brand-name drug whose patent has expired

a medication for aciphex manufacturer purchase aciphex which the original manufacturer has aciphex manufacturer lost patent protection

a medication whose active ingredients, safety, dosage, quality and strength are identical to that of its brand - name counterpart

a non-branded copy of a branded drug, and is supposed to be an identical, or 'bio-equivalent' copy

a pharmaceutical product, which is the chemical and therapeutic equivalent of a brand-name drug as to which the patent and/or market exclusivity has expired

a product that the FDA has found to be bioequivalent to a brand name drug

A drug which is the pharmaceutical equivalent to one or more brand name drugs. Such generic drugs have been approved by the Food and Drug Administration as meeting the same standards of safety, purity, strength, dosage form and effectiveness as the brand drug. back to the top

A prescription drug that is chemically equivalent to a brand name drug dispensed under its generic chemical name. Generic drugs are cheaper versions of expensive brand name drugs with the same active ingredients, strength and dosage form.

nbspDrugs, which have been approved by the FDA to be bioequivalent to Brand Name Drugs and are not manufactured or marketed under a registered trade name or trademark. Generic Drugs must meet the same FDA specifications for safety, purity and potency and must be dispensed in the dame dosage form as the counterpart Brand Name Drug.

Any chemically equivalent reproduction of a Brand Name Medication whose patent has expired.

A generic drug is the same as a brand name drug in dosage, safety, strength, how it is taken, quality, performance, and intended use. Before approving a generic drug product, FDA requires many rigorous tests and procedures to assure that the generic drug can be substituted for the brand name drug. The FDA bases evaluations of substitutability, or " therapeutic equivalence," of generic drugs on scientific evaluations. By law, a generic drug product must contain the identical amounts of the same active ingredient(s) as the brand name product. Drug products evaluated as "therapeutically equivalent" can be expected to have equal effect and no difference when substituted for the brand name product.

means a Prescription Drug, which has the equivalency of the brand name drug with the same use and metabolic disintegration. This Plan will consider as a Generic Drug any Food and Drug Administration approved generic pharmaceutical dispensed according to the professional standards of a licensed pharmacist and clearly designated by the pharmacist as being generic.

Prescription drugs that have the same active ingredient formula as brand-name drugs. Generic drugs usually cost less than brand-name drugs and are required by the Food and Drug Administration (FDA) to be as safe and as effective as the brand-name drug.

A classification of prescription that requires a lesser co-pay because of patent or cost of producing the drug.

a pharmaceutical product, usually intended to be interchangeable with the innovator product, which is generally manufactured without a licence from the innovator company, and marketed after the expiry of patent or other exclusivity rights. Generic drugs are marketed either under a non-proprietary or approved name, rather than a proprietary or brand name

A drug that is the generic, biological equivalent of a brand-name drug. Generic drugs must contain the same active ingredients as the brand name, and must deliver the same amount of medicine into the body in the same way. In most cases, generic drugs can be substituted for brand names without physician approval.

the chemical equivalent to a "brand name drug." These drugs cost less, and the savings is passed onto health plan members in the form of a lower co-pay.

A drug that is not sold under a brand name; for example, carbamazepine can be obtained as a generic drug or as Tegretol or Carbatrol, its brand names.

A medicinal product with the same active ingredient, but not necessarily the same inactive ingredients as a brand-name drug. A generic drug may only be marketed after the original drug's patent has expired.

The identical or bioequivalent medicine to a brand name drug in dosage form, safety, strength, route of administration, quality, performance characteristics and intended use; although generic drugs are chemically identical to their branded counterparts, they are typically sold at substantial discounts from the branded price.

A prescription drug that has the same active-ingredient formula as a brand name drug. Generic drugs usually cost less than brand name drugs and are rated by the Food and Drug Administration (FDA) to be as safe and effective as brand name drugs.

A prescription drug which has the same active-ingredient formula as a brand-name drug. A generic drug is known only by its formula name and its formula is available to any pharmaceutical company. Generic drugs are rated by the Food and Drug Administration (FDA) to be as safe and as effective as brand-name drugs and are typically less costly.

A prescription drug which is not protected by trademark registration, but is produced and sold under the chemical formulation name.

A prescription that is not protected by a drug patent. A generic medication is basically a copy of the brand name drug. A generic drug may have a different color or shape than its brand name counterpart, but it must have the same active ingredients, strength, and dosage form (i.e., pill, liquid, or injection), and provide the same effectiveness and safety. Generics generally cost less than brand name drugs.

a drug that does not have the trademark of the original manufacturer. It is chemically identical to and generally costs less than its brand name counterpart.

A medication that has the same active ingredients, is available in the same strength and dosage form, and is administered in the same way as its equivalent brand-name drug. Generics are usually less costly than brand-name equivalents.

A generic medication is an equivalent of a brand name drug. A generic drug provides the same effectiveness and safety as a brand name drug and usually costs less. A generic drug may have a different color or shape than its brand name counterpart, but it must have the same active ingredients, strength, and dosage form (pill, liquid, or injection).

A drug which is a "twin" to a brand name drug and which is allowed to be produced after the brand name drug's patent has expired. It is also called a "generic equivalent."

A medicine that has the same active drug as a trademarked brand-named version. Generic drugs usually cost less than their brand-name versions.

the version of an approved drug produced by a competitor after a pioneer firm's patents expire.

A chemically equivalent copy designed from a brand-name drug that has an expired patent. A generic is typically less expensive and sold under a common or "generic" name for that drug, not the name brand.

a drug whose patent has expired thus enabling it to be manufactured by any company

A commonly used term to identify non-brand name drugs that are sold. Typically, generic drugs are sold at a lower cost than brand name drugs. A generic drug is a pharmaceutical equivalent to another drug and has identical strength, dosage form, and concentration.

A drug which is the same as a brand name drug and which is allowed to be produced after the brand name drug's patent has expired.

Drugs sold under a general simplified chemical name rather than a brand name. Available generic drugs are no longer under patent restrictions. A generic drug contains exactly the same active ingredient as its corresponding brand-name counterpart. Usually drugs are produced generically if there is a large market for the drug.

A generic drug is a prescription drug with the same active-ingredient formula as a brand-name drug. Generic drugs are rated by the Food and Drug Administration to be as safe and effective as brand-name drugs and usually cost less.

A drug that is sold under its chemical name. Generic drugs are required by law to meet the same standards of purity, effectiveness, and strength, and they are usually less expensive than their brand name drug counterpart.

A drug that is the pharmaceutical equivalent to a Brand Name Drug. The Food and Drug Administration have approved such generic drugs as meeting the same standards of safety, purity, strength and effectiveness as the brand drug.

A copy of a brand-name drug that is no longer protected by a patent. Generic drugs typically contain the same active ingredients as brand-name originals and are usually as effective as, but less expensive than, brand-name originals. Your copayment is less when you purchase generic drugs.

is a prescription drug which is a chemical equivalent copy of a Brand-Name drug. Generic drugs are formulated upon a manufacturer's Brand-Name drug patent expiration. Generic drugs are usually less expensive than branded drugs and are usually sold by their chemical formula or "generic" name. For example, Valium is a Brand-Name drug, whereas Diazepam is its chemically equivalent generic.

A drug known by its chemical name rather than by a brand name.

A chemically equivalent copy designed from a brand-name drug whose patent has expired (typically less expensive and sold under the common name).

A "twin" to a "brand name drug" once the brand name company's patent has run out and other drug companies are allowed to sell a duplicate of the original. Generic drugs are cheaper, and most prescription and health plans reward clients for choosing generics.

A pharmaceutical product usually intended to be interchangeable with the innovator product, which is not protected by a patent in the country or is licensed. Generic drugs are marketed either under a non-proprietary or approved name rather than a proprietary name.

A drug chemically equivalent to brand drugs but not produced or marketed after the brand drug's patent has expired. They are generally priced significantly lower than brand drugs.

A "twin" to a brand name drug available once the brand name company's patent has expired and other drug companies are allowed to sell a duplicate of the original. Generic drugs are usually less expensive than brand name drugs.

A drug product produced and marketed under its chemical or common name. This can only be done after a proprietary drug goes off patent after 17 years. While generic drugs are less expensive for consumers, they must still meet the stringent standards of cGMPâ€(tm)s as specified in the FDA CDER.

A generic drug (pl. generic drugs, short: generics) is a drug which is bioequivalent to a brand name drug with respect to pharmacokinetic and pharmacodynamic properties. These drugs are usually sold at a lower price than the brand name drug. Generic medicines must contain the same active ingredient at the same strength as the "innovator" brand, be bioequivalent, and are required to meet the same pharmacopoeial requirements for the preparation.