Drug Master Files for: oxytetracycline hydrochloride
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oxytetracycline hydrochloride Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 11650 | A | II | 9/8/1995 | HUASHU PHARMACEUTICAL CORP | OXYTETRACYCLINE BASE |
| 13200 | I | II | 4/30/1998 | COMPANHIA INDUSTRIAL PRODUTORA DE ANTIBIOTICOS SARL | OXYTETRACYCLINE |
| 13302 | I | II | 9/1/1998 | PFIZER | OXYTETRACYCLINE |
| 13305 | I | II | 9/1/1998 | IBI | OXYTETRACYCLINE |
| 13312 | I | II | 9/1/1998 | DIASPA TRADE MARK STRIDES ITALIA SRL | OXYTETRACYCLINE HYDROCHLORIDE |
| 13313 | I | II | 9/1/1998 | DIASPA TRADE MARK STRIDES ITALIA SRL | OXYTETRACYCLINE |
| 13322 | I | II | 9/1/1998 | PFIZER INC | OXYTETRACYCLINE |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
