Drug Master Files for: CLARITHROMYCIN
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CLARITHROMYCIN Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
14766 | I | II | 3/10/2000 | XIAN PHARMACEUTICAL FACTORY | CLARITHROMYCIN |
15276 | A | II | 2/6/2001 | TEVA PHARMACEUTICAL INDUSTRIES LTD | CLARITHROMYCIN USP |
15615 | I | II | 9/6/2001 | FERMIC SA DE CV | CLARITHROMYCIN |
16083 | I | II | 8/6/2002 | SANDOZ INDUSTRIAL PRODUCTS SA | CLARITHROMYCIN (NON-STERILE BULK) |
16218 | I | II | 10/30/2002 | WOCKHARDT LTD | CLARITHROMYCIN |
16518 | A | II | 4/8/2003 | IND SWIFT LABORATORIES LTD | CLARITHROMYCIN |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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