Generated: January 22, 2018
DrugPatentWatch Database Preview
Drug Master Files for: CAPTOPRIL; HYDROCHLOROTHIAZIDE
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|3681||I||II||12/5/1979||FOREST LABORATORIES INC||CAPTOPRIL-F 250MG C.R. TABLETS|
|3687||I||II||12/5/1979||FOREST LABORATORIES INC||CAPTOPRIL-S 250MG C.R. TABLETS|
|5958||I||II||8/15/1985||KV PHARMACEUTICAL CO||CAPTOPRIL TABLETS, 100MG.|
|8460||A||II||3/5/1990||QUIMICA SINTETICA SA||CAPTOPRIL|
|9221||I||II||7/3/1991||EGIS PHARMACEUTICALS PRIVATE LTD||CAPTOPRIL|
|9745||I||II||6/23/1992||SHANDONG WEI FANG PHARMACEUTICAL FACTORY||CAPTOPRIL|
|11228||I||II||12/16/1994||BORYUNG PHARMACEUTICAL CO LTD||CAPTOPRIL|
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Drug Master File Glossary
STATUS OF DMFS
- A = Active. This means that the DMF was found acceptable for filing, administratively, and is up-to-date.
- I = Inactive
- N = Not an assigned number
- P = DMF Pending Filing Review
TYPES OF DMFs
- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)
- Type II Drug Substance, Drug Substance Intermediate, and Material Used in Their Preparation, or Drug Product
- Type III Packaging Material
- Type IV Excipient, Colorant, Flavor, Essence, or Material Used in Their Preparation
- Type V FDA Accepted Reference Information
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