Drug Master Files for: DEMECLOCYCLINE HYDROCHLORIDE
DEMECLOCYCLINE HYDROCHLORIDE Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 13330 | I | II | 9/1/1998 | WYETH PHARMACEUTICALS | DEMECLOCYCLINE HYDROCHLORIDE |
| 13403 | I | II | 9/1/1998 | FERMIC SA DE CV | DEMECLOCYCLINE HYDROCHLORIDE |
| 13604 | I | II | 9/1/1998 | LEDERLE LABORATORIES | DEMECLOCYCLINE HYDROCHLORIDE |
| 13605 | I | II | 9/1/1998 | LEDERLE LABORATORIES | DEMECLOCYCLINE |
| 13744 | A | II | 9/1/1998 | CKD BIO CORP | DEMECLOCYCLINE HYDROCHLORIDE |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
