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- ...fda.gov/BiologicsBloodVaccines/BloodBloodProducts/ Blood & Blood Products. Food and Drug Administration</ref>. As well as being a regulatory agency, it both does research and work | publisher = Food and Drug Administration}}</ref>Until her confirmation, the FDA was under the interim leadership of40 KB (5,751 words) - 04:07, 19 September 2013
- *[[Food and Drug Administration/Catalogs/Therapeutic Equivalence Code|Therapeutic Equivalence Code]]113 bytes (12 words) - 04:31, 13 July 2010
- 139 bytes (20 words) - 04:08, 19 September 2013
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- Auto-populated based on [[Special:WhatLinksHere/Food and Drug Administration]]. Needs checking by a human.4 KB (505 words) - 16:36, 11 January 2010
- * [http://www.fda.gov/ Food and Drug Administration Home Page] ...s.html Biologics Centennial: 100 Years of Biologics Regulation] — from the Food and Drug Administration Home Page524 bytes (76 words) - 04:08, 19 September 2013
- #REDIRECT [[Food and Drug Administration/Catalogs/Therapeutic Equivalence Code]]80 bytes (9 words) - 04:29, 13 July 2010
- ...uivalence Code for [[generic drug]]s by the [[United States of America]] [[Food and Drug Administration]]. The table is from: http://www.fda.gov/Drugs/DevelopmentApprovalProcess/F14 KB (1,981 words) - 13:19, 2 February 2023
Page text matches
- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=079013 Drugs@FDA]. U S Food and Drug Administration</ref>1 KB (142 words) - 11:47, 2 February 2023
- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=077451 Drugs@FDA]. U S Food and Drug Administration</ref>1 KB (142 words) - 14:35, 2 February 2023
- * [http://www.fda.gov/ Food and Drug Administration Home Page] ...s.html Biologics Centennial: 100 Years of Biologics Regulation] — from the Food and Drug Administration Home Page524 bytes (76 words) - 04:08, 19 September 2013
- #REDIRECT [[Food and Drug Administration/Catalogs/Therapeutic Equivalence Code]]80 bytes (9 words) - 04:29, 13 July 2010
- {{r|Food and Drug Administration}}428 bytes (54 words) - 18:09, 10 January 2010
- * [http://dailymed.nlm.nih.gov/ DailyMed]. Drug information approved by the [[Food and Drug Administration]].732 bytes (100 words) - 07:40, 8 September 2008
- ...Biomarkers in the Context of Approved Drug Labels. U.S. [[Food and Drug Administration]].423 bytes (56 words) - 13:18, 24 July 2008
- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=075310 Drugs@FDA]. U S Food and Drug Administration</ref>1 KB (163 words) - 14:10, 9 October 2009
- ...gs@FDA |author= |authorlink= |coauthors= |date= |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-02-02 KB (233 words) - 11:54, 2 February 2023
- ...gs@FDA |author= |authorlink= |coauthors= |date= |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-01-2784 bytes (100 words) - 14:12, 2 February 2023
- *[[Food and Drug Administration/Catalogs/Therapeutic Equivalence Code|Therapeutic Equivalence Code]]113 bytes (12 words) - 04:31, 13 July 2010
- ...delayed release brand of omeprazole was approved for AstraZeneca by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve2 KB (199 words) - 14:07, 2 February 2023
- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=040422 Drugs@FDA]. U S Food and Drug Administration</ref>3 KB (410 words) - 11:51, 2 February 2023
- The U.S. regulatory process under which the [[Food and Drug Administration]] authorizes the marketing of new drugs, for which it has verified safety a298 bytes (42 words) - 14:43, 4 October 2008
- ...brand of rosuvastatin was approved for Merck and Schering-Plough by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve2 KB (265 words) - 14:07, 2 February 2023
- ...|homeopathic physician]] and educator; drafted legislation creating U.S. [[Food and Drug Administration]] giving special exemptions to homeopathy320 bytes (39 words) - 13:58, 20 March 2023
- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=076588 Drugs@FDA]. U S Food and Drug Administration</ref> ...this usage is approved by the [[United States of America|United States]] [[Food and Drug Administration]].<ref name="pmid18541820">{{cite journal| author=Cernik C, Gallina K, Br4 KB (502 words) - 14:34, 2 February 2023
- {{r|Food and Drug Administration}}764 bytes (100 words) - 16:05, 11 January 2010
- ...one-proguanil''', made by [[Smith Kline Glaxo]] and approved by the U.S. [[Food and Drug Administration]] in 2000, is a fixed-combination [[antimalarial]] drug for [[chemoprophyla1 KB (171 words) - 15:29, 27 May 2010
- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=076436 Drugs@FDA]. U S Food and Drug Administration</ref>3 KB (403 words) - 13:22, 2 February 2023
- [[Drug toxicity]] includes arrhythmias. The [[United States of America]] [[Food and Drug Administration]] has issued a warning to not use higher doses because of use of the [[cyto1 KB (123 words) - 11:44, 2 February 2023
- {{r|Food and Drug Administration}}1 KB (150 words) - 19:29, 11 January 2010
- In the [[United States of America]], the [[Food and Drug Administration]] provides regulation:1 KB (179 words) - 11:46, 2 February 2023
- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=016418 Drugs@FDA]. U S Food and Drug Administration</ref> ...rchType=BasicSearch&Search_Button=Submit&searchTerm=070103 Drugs@FDA]. U S Food and Drug Administration</ref>2 KB (236 words) - 14:07, 2 February 2023
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- {{r|Food and Drug Administration}}716 bytes (94 words) - 13:09, 10 February 2023
- {{r|Food and Drug Administration}}865 bytes (110 words) - 17:00, 11 January 2010
- Within the regulatory authority of the U.S. Food and Drug Administration, '''radiation-emitting product''' has a specific technical and legal meanin | author = Center for Diagnostics and Radiologic Health, [[Food and Drug Administration]], [[U.S. Department of Health and Human Services]]}}</ref>2 KB (318 words) - 06:05, 31 May 2009
- Viread brand of tenofovir was approved for Gilead Sciences by the [[Food and Drug Administration]] in the [[United States of America|United States]] with a [http://www.fda.2 KB (335 words) - 14:35, 2 February 2023
- {{r|Food and Drug Administration}}994 bytes (123 words) - 16:54, 11 January 2010
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- The drug is approved by the U.S. [[Food and Drug Administration]] for [[depression]], [[generalized anxiety disorder]], [[obsessive-compuls2 KB (279 words) - 11:00, 10 February 2010
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- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=074047 Drugs@FDA]. U S Food and Drug Administration</ref>3 KB (394 words) - 07:05, 17 October 2009
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- ...uthor=Anonymous |authorlink= |coauthors= |date= |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-02-0 ...ts |author= |authorlink= |coauthors= |date=2009 |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-01-25 KB (657 words) - 23:50, 12 July 2010
- ...dication]] that is a [[antineoplastic agent]]. It is approved by the U.S. Food and Drug Administration for the palliative treatment [[chronic lymphocytic leukemia]] (CLL). It is638 bytes (88 words) - 02:54, 10 February 2010
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- Remeron brand of mirtazapine was approved for Organon USA by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve3 KB (422 words) - 14:08, 2 February 2023
- {{r|Food and Drug Administration}}508 bytes (65 words) - 18:03, 11 January 2010
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- ...UMARATE&SponsorApplicant=MUTUAL%20PHARM&ProductMktStatus=3 Drugs@FDA]. U S Food and Drug Administration</ref>2 KB (313 words) - 14:09, 4 July 2009
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