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Saccharomyces boulardii Eligibility for Consideration To Be Added to the Over-the-Counter Drug Monograph for Antidiarrheal Drug Products; Request for Safety and Effectiveness Data; Withdrawal - 10/27 - 05:13 PM ET

Saccharomyces boulardii Eligibility for Consideration To Be Added to the Over- the-Counter Drug Monograph for Antidiarrheal Drug Products; Request for Safety and Effectiveness Data; Withdrawal - 10/27 - 09:12 AM ET

FDA Warns of Unapproved and Illegal H1N1 Drug Products Purchased Over the Internet - 10/15 - 03:58 PM ET

Draft Guidance for Industry on Microbiological Data for Systemic Antibacterial Drug Products--Development, Analysis, and Presentation; Availability - 09/17 - 08:22 AM ET

FDA News Release: FDA Issues Warning Letters to Marketers of Topical Ibuprofen Drug Products - 08/20 - 06:45 PM ET

Research and Markets: With Ever-Evolving Best Practice and Guidelines on Leachables & Extractables, This Conference Was a One-Stop Source of Current Information on the Topic - 07/16 - 04:09 AM ET

Research and Markets: Product Commercialization Excellence: Preparation and Management of Fixed-Dose Combination Drug Products - 07/15 - 06:24 AM ET

Guidance for Industry on Updating Labeling for Susceptibility Test Information in Systemic Antibacterial Drug Products and Antimicrobial Susceptibility Testing Devices; Availability - 07/02 - 11:13 AM ET

Organ-Specific Warnings; Internal Analgesic, Antipyretic, and Antirheumatic Drug Products for Over-the-Counter Human Use; Final Monograph; Corrections - 06/30 - 08:48 AM ET

US Food & Drug Administration: U.S. Marshals Seize Drug Products Manufactured by Caraco Pharmaceutical Laboratories Ltd. - 06/26 - 12:04 PM ET

FDA News Release: U.S. Marshals Seize Drug Products Manufactured by Caraco Pharmaceutical Laboratories Ltd. - 06/26 - 03:08 AM ET

FDA OKs injectable ibuprofen - 06/15 - 09:54 AM ET

Determination That THORAZINE (Chlorpromazine Hydrochloride) Injection and 18 Other Drug Products Were Not Withdrawn From Sale for Reasons of Safety or Effectiveness - 06/13 - 02:42 PM ET

US Food & Drug Administration: FDA Approves Injectable Form of Ibuprofen - 06/12 - 05:58 AM ET

Determination That DECADRON Tablets and Nine Other Drug Products Were Not Withdrawn From Sale for Reasons of Safety or Effectiveness - 05/14 - 09:55 AM ET

Compliance Guidance for Small Business Entities on Labeling Over-the-Counter Human Drug Products; Availability - 05/13 - 09:12 AM ET

Draft Guidance for Industry on Label Comprehension Studies for Nonprescription Drug Products; Availability - 05/01 - 12:02 PM ET

Organ-Specific Warnings; Internal Analgesic, Antipyretic, and Antirheumatic Drug Products for Over-the-Counter Human Use; Final Monograph - 04/29 - 11:16 AM ET

Neilgen Pharma Inc. and Advent Pharmaceutical Recall All Prescription Cough and Cold Drug Products Sold on or after March 5, 2008 (April 20) - 04/21 - 04:01 PM ET

Sodium Shale Oil Sulfonate Eligibility for Inclusion in Monograph; Over-the-Counter Dandruff, Seborrheic Dermatitis, and Psoriasis Drug Products for Human Use; Request for Safety and Effectiveness Data - 04/07 - 05:27 PM ET

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