Generic prescription drug definition

Generic prescription drug means a prescription drug, whether identified by its chemical, proprietary, or nonproprietary name, that is accepted by the U.S. Food and Drug Administration as therapeutically equivalent and interchangeable with drugs having an identical amount of the same active ingredient and so indicated by Medispan or any other publication designated by Aetna.
Sample 1Sample 2Sample 3
Generic prescription drug means a Prescription Drug that is produced by more than one manufacturer. It is chemically the same as and usually costs less than the Brand Name Prescription Drug for which it is being substituted.
Sample 1
Generic prescription drug means a Prescription Drug that is produced by more than one manufacturer. It is chemically the same as and usually costs less than the Non-Formulary or Formulary Drug for which it is being substituted.
Sample 1

Examples of Generic prescription drug in a sentence

  • The Clean Water Act provides that a state program must have adequate authority "to abate violations of the permit or the permit program, including civil and criminal penalties and other ways and means of enforcement." See 33 U.S.C. § 1342 (b)(2)(b)(7).

  • Generic prescription drug manu- facturers, on the other hand, received a l80-day exclusivity period, awarded to the first company to successfully chal- lenge a brand name patent and enter the market.This 6-month exclusivity period hasbeen crucial to encouraging generic drug companies to make existing drugs more affordable.

  • Conti et al, Generic prescription drug price increases: which products will be affected by proposed anit- gouging legislation?”, page 4-5.

  • Any proposals received after the time and date above may, at the District’s sole discretion of the District, be returned unopened or set aside without consideration.

  • Generic prescription drug includes a prescription drug: (1) that is chemically equivalent to a brand drug; or (2) that UnitedHealthcare (UHC) identifies as a generic based on available data resources including, but not limited to, the daily Medi-Span file load memo that classifies drugs as either brand or generic based on a number of factors.

  • This means we need to be familiar with declarations, action plans and statements concerning HRH.

  • In other words, we assume that when prices charged by the two firms are identical, switchers employ an exogenous cue to break ties and purchase from one of the two firms.

  • Generic prescription drug dispensary with no controlled substances or over-the-counter medications.The proposal must include all three services to be considered.The proposed center will not offer occupational health services like worker’s comp, work-related employee physicals or drug screens.Proposal Elements: Proposals shall contain the following: General Information 1.

  • Generic prescription drug development; Generic manufacturers invest three to six years and anestimated $ 4 million to bring a new generic drug to market.

  • Those changes are as follows: Generic prescription drug increase from $3 to $5; non-generic (brand) prescription drug increase from $15 to $20; co-pay increase from $10 to $20.

Related to Generic prescription drug

  • Prescription drug means any drug required by federal law or regulation to be dispensed only

  • Prescription drugs means drugs, medicine and controlled substances which by law can only be prescribed for human use by persons authorized by law.

  • Prescription drug order means a lawful order of a practitioner for a drug or device for a specific patient that is communicated to a pharmacist.

  • Nonprescription drug or "over-the-counter drug" means any

  • Nonprescription drugs means nonnarcotic medicines or drugs which may be sold without a prescription and are prepackaged and labeled for use by the consumer in accordance with the requirements of the statutes and regulations of this state and the federal government;

  • Drug means (i) articles or substances recognized in the official United States Pharmacopoeia

  • Participating Prescription Drug Provider means an independent retail Pharmacy, chain of retail Pharmacies, mail-order Pharmacy or specialty drug Pharmacy which has entered into an agreement to provide pharmaceutical services to participants in the benefit program. A retail Participating Pharmacy may or may not be a select Participating Pharmacy as that term is used in the Vaccinations Obtained Through Participating Pharmacies section.

  • Drug abuse means any pattern of pathological use of drugs that causes impairment in social or occupational functioning, or that produces physiological dependency evidenced by physical tolerance or by physical symptoms when it is withdrawn.

  • Drug addiction means a disease characterized by a

  • Generic Drug means any Prescription Drug approved by the FDA that has the same bio-equivalency as a specific Brand Name Drug.

  • Prescription means an order for drugs or medical supplies, written or signed or transmitted by word

  • Brand Name Drug means a Prescription Drug that has been given a name by a manufacturer or distributor to distinguish it as produced or sold by a specific manufacturer or distributor and may be used and protected by a trademark.

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Biological safety cabinet means a containment unit suitable for the preparation of low to moderate risk agents where there is a need for protection of the product, personnel, and environment, according to National Sanitation Foundation (NSF) Standard 49.

  • Licensed clinical social worker means an individual who meets the licensed clinical social worker requirements established in KRS 335.100.

  • Participating Clinical Laboratory means a Clinical Laboratory which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • New drug means: (i) any drug, except a new animal drug or an animal feed bearing or containing

  • New Drug Application means a New Drug Application filed with the FDA in accordance with Applicable Law.

  • FDA means the United States Food and Drug Administration.

  • Tobacco product means any substance containing tobacco leaf, including but not limited to, cigarettes, cigars, pipe tobacco, hookah tobacco, snuff, chewing tobacco, dipping tobacco, bidis, blunts, clove cigarettes, or any other preparation of tobacco; and any product or formulation of matter containing biologically active amounts of nicotine that is manufactured, sold, offered for sale, or otherwise distributed with the expectation that the product or matter will be introduced into the human body by inhalation; but does not include any cessation product specifically approved by the U.S. Food and Drug Administration for use in treating nicotine or tobacco dependence.

  • Biologics License Application or “BLA” means an application requesting permission from the FDA to introduce, or deliver for introduction, a biological product into interstate commerce, or any similar application or submission for marketing authorization of a product filed with a Regulatory Authority to obtain Regulatory Approval for such product in a country or group of countries.

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

  • Anti-Static Product means a product that is labeled to eliminate, prevent, or inhibit the accumulation of static electricity. “Anti-Static Product” does not include “Electronic Cleaner,” “Floor Polish or Wax,” “Floor Coating,” and products that meet the definition of “Aerosol Coating Product” or “Architectural Coating.”

  • Approved clinical trial means a phase I, phase II, phase III, or phase IV clinical trial that is conducted in relation to the prevention, detection, or treatment of cancer or other life-threatening disease or Condition and is described in any of the following:

  • Active Pharmaceutical Ingredient or “API” shall mean one or more of the following active pharmaceutical ingredients: tenofovir alafenamide (“TAF”), tenofovir disoproxil fumarate (“TDF”), elvitegravir (“EVG”), and cobicistat (“COBI”).

  • Phase III Clinical Trials means a Clinical Trial for the Product on sufficient numbers of patients to generate safety and efficacy data to support Regulatory Approval in the proposed therapeutic indication, conducted in accordance with current good clinical practices and in accordance with a protocol that has been reviewed by the FDA and reflects any comments or concerns raised by the same.