Drug Master Files for: clindamycin palmitate hydrochloride
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clindamycin palmitate hydrochloride Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
12886 | I | II | 2/28/1998 | SUZHOU NUMBER 4 PHARMACEUTICAL FACTORY | CLINDAMYCIN HYDROCHLORIDE ETHANOLATE INTERMEDIATE |
12922 | A | II | 4/2/1998 | TRIFARMA SPA | CLINDAMYCIN PHOSPHATE USP |
12988 | I | II | 5/15/1998 | SUZHOU NUMBER 4 PHARMACEUTICAL FACTORY | CLINDAMYCIN ISOPROPYLIDENE, INTERMEDIATE |
13082 | A | II | 7/8/1998 | ZHEJIANG CANDORLY PHARMACEUTICAL CO LTD | CLINDAMYCIN PHOSPHATE U.S.P. |
13371 | I | II | 9/1/1998 | PFIZER INC | CLINDAMYCIN HYDROCHLORIDE |
13412 | A | II | 9/1/1998 | PHARMACIA AND UPJOHN SUB PFIZER INC | CLINDAMYCIN PALMITATE HYDROCHLORIDE USP KALAMAZOO |
>DMF No. | >Status | >Type | >Submission Date | >Holder | >Subject |
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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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