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• Generic drug
  ...al companies." <ref>{{MeSH}}</ref> Government agencies determine whether a generic drug is [[bioequivalence|bioequivalent]] to a [[brand]] name drug with respect t ...randed generic may be an authorized generic (see description of authorized generic drug below).
  18 KB (2,553 words) - 13:17, 2 February 2023
• Generic drug/Definition
  175 bytes (23 words) - 17:49, 14 May 2010
• Generic drug/Approval
  12 bytes (1 word) - 13:55, 26 September 2007
• Generic drug/Related Articles
  Auto-populated based on [[Special:WhatLinksHere/Generic drug]]. Needs checking by a human.
  592 bytes (75 words) - 16:48, 11 January 2010

Page text matches

• Adderall/Definition
  ...ly for [[attention deficit hyperactivity disorder]]; also available as a [[generic drug]]
  189 bytes (24 words) - 19:06, 29 January 2010
• Pharmacology/Related Articles
  {{r|Generic drug}}
  1 KB (150 words) - 19:29, 11 January 2010
• Drug industry
  ...t.cfm Orange Book] summarizes evaluations of therapeutic equivalence for [[generic drug]]s.
  1 KB (179 words) - 11:46, 2 February 2023
• Azithromycin
  ...url= |archivedate= |quote= |accessdate=2009-02-01}}</ref> Non-authorized [[generic drug]]s manufactured by [http://www.tevapharm.com/ Teva], [http://www.sandoz.com
  2 KB (233 words) - 11:54, 2 February 2023
• Bioequivalence/Related Articles
  {{r|Generic drug}}
  489 bytes (62 words) - 11:22, 11 January 2010
• Generic drug/Related Articles
  Auto-populated based on [[Special:WhatLinksHere/Generic drug]]. Needs checking by a human.
  592 bytes (75 words) - 16:48, 11 January 2010
• Propranolol
  [[Generic drug|Generic]] propranolol was available October 22, 1985.<ref>[http://www.acces
  2 KB (236 words) - 14:07, 2 February 2023
• Bioequivalence
  ...ts, 53% of published editorials on the topic "expressed a negative view of generic drug substitution". ...01}}</ref> The approval process for generic drugs began in the late 1960s. Generic drug manufacturers are required to prove that their formulation exhibits bioequi
  5 KB (657 words) - 23:50, 12 July 2010
• Patent/Related Articles
  {{r|Generic drug}}
  335 bytes (41 words) - 14:40, 16 September 2010
• Trademark/Related Articles
  {{r|Generic drug}}
  1 KB (138 words) - 21:03, 11 January 2010
• Bisoprolol
  ...rview&DrugName=ZEBETA Drugs@FDA]. U S Food and Drug Administration</ref> [[Generic drug|Generic]] bisoprolol was approved in 2002.<ref>[http://www.accessdata.fda.g
  2 KB (313 words) - 14:09, 4 July 2009
• Pharmacokinetics/Related Articles
  {{r|Generic drug}}
  520 bytes (65 words) - 19:29, 11 January 2010
• Smoking cessation/Related Articles
  {{r|Generic drug}}
  592 bytes (76 words) - 20:26, 11 January 2010
• Generic drug
  ...al companies." <ref>{{MeSH}}</ref> Government agencies determine whether a generic drug is [[bioequivalence|bioequivalent]] to a [[brand]] name drug with respect t ...randed generic may be an authorized generic (see description of authorized generic drug below).
  18 KB (2,553 words) - 13:17, 2 February 2023
• Food and Drug Administration/Related Articles
  {{r|Generic drug}}
  4 KB (505 words) - 16:36, 11 January 2010
• Medication
  ...cine]]. Those that are not patented (or with expired patents) are called [[generic drug]]s since they can be produced by other companies without restrictions or li
  7 KB (977 words) - 08:20, 11 April 2024
• Food and Drug Administration/Catalogs/Therapeutic Equivalence Code
  The following table provides the Therapeutic Equivalence Code for [[generic drug]]s by the [[United States of America]] [[Food and Drug Administration]]. Th
  14 KB (1,981 words) - 13:19, 2 February 2023
• Cephalosporin
  ...gested by the [[World Health Organization]] use the "cef" spelling for the generic drug name of all cephalosporins.
  3 KB (284 words) - 21:37, 2 May 2010
• Atenolol
  [[Generic drug|Generic]] atenolol was available in 1988.<ref>[http://www.accessdata.fda.go
  16 KB (2,243 words) - 11:52, 2 February 2023
• Food and Drug Administration
  ...Generic Drugs] (OGD) is responsible for certifying [[bioequivalence]] of [[generic drug]]s. The [http://www.fda.gov/cder/ob/ Orange Book] contains all approved bi ...sh to produce generic versions of off-patent, previously approved drugs. [[Generic drug]] manufacturers are only required to show that the active ingredient in the
  40 KB (5,751 words) - 04:07, 19 September 2013