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Abbreviated New Drug Applications: Impurities in Drug Products 11/29/2010
Alternate Source of Active Pharmaceutical Ingredients in Pending ANDAs (I) 12/12/2000
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ANDAs: Pharmaceutical Solid Polymorphism; Chemistry, Manufacturing and Controls Information (I) 7/9/2007
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Individual Product Bioequivalence Recommendations - List of Product Bioequivalence Recommendations (I) 6/11/2010
Letter announcing that the OGD will now accept the ICH long-term storage conditions as well as the stability studies conducted in the past (I)8/18/1995
Letter describing efforts by the CDER & the ORA to clarify the responsibilities of CDER chemistry review scientists and ORA field investigators in the new & abbreviated drug approval process in order to reduce duplication or redundancy in the process (I) 10/14/1994
Letter on incomplete Abbreviated Applications, Convictions Under GDEA, Multiple Supplements,Annual Reports for Bulk Antibiotics, Batch Size for Transdermal Drugs, Bioequivalence Protocols, Research, Deviations from OGD Policy (I) 4/8/1994
Letter on the provision of new information pertaining to new bioequivalence guidelines and refuse-to-file letters (I) 7/1/1992
Letter on the provision of new procedures and policies affecting the generic drug review process (I) 3/15/1989
Letter on the request for cooperation of regulated industry to improve the efficiency and effectiveness of the generic drug review process, by assuring the completeness and accuracy of required information and data submissions (I) 11/8/1991
Letter on the response to 12/20/84 letter from the Pharmaceutical Manufacturers Association about the Drug Price Competition and Patent Term Restoration Act (I) 3/26/1985
Letter to all ANDA and AADA applicants about the Generic Drug Enforcement Act of 1992 (GDEA), and the Office of Generic Drugs intention to refuse-to-file incomplete submissions as required by the new law (I) 1/15/1993
Letter to regulated industry notifying interested parties about important detailed information regarding labeling, scale-up, packaging, minor/major amendment criteria, and bioequivalence requirements (I) 8/4/1993
Major, Minor, and Telephone Amendments to Abbreviated New Drug Applications (I) 12/21/2001
Revising ANDA Labeling Following Revision of the RLD Labeling (I) 4/25/2000
Size, Shape, and Other Physical Attributes of Generic Tablets and Capsules 12/10/2013
Submission of Summary Bioequivalence Data for Abbreviated New Drug Applications (I) 5/6/2011
Variations in Drug Products that May Be Included in a Single ANDA (I) 1/27/1999
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