Drug Master Files for: tetracycline hydrochloride
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tetracycline hydrochloride Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
1024 | I | 12/6/1966 | MURRAY E CORN ASSOC INC | TETRACYCLINE HCL S.R. | |
11650 | A | II | 9/8/1995 | HUASHU PHARMACEUTICAL CORP | OXYTETRACYCLINE BASE |
11917 | I | II | 4/9/1996 | BOEHRINGER MANNHEIM SA | 4-EPITETRACYCLINE HYDROCHLORIDE |
13200 | I | II | 4/30/1998 | COMPANHIA INDUSTRIAL PRODUTORA DE ANTIBIOTICOS SARL | OXYTETRACYCLINE |
13288 | I | II | 9/1/1998 | SQUIBB | TETRACYCLINE HYDROCHLORIDE |
13300 | I | II | 9/1/1998 | PFIZER INC | TETRACYCLINE |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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