Drug Master Files for: pioglitazone hydrochloride
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pioglitazone hydrochloride Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 16635 | A | II | 6/11/2003 | BIOCON LTD | PIOGLITAZONE HYDROCHLORIDE USP |
| 16672 | A | II | 6/30/2003 | CIPLA LTD | PIOGLITAZONE HYDROCHLORIDE USP |
| 16675 | I | II | 7/2/2003 | DR REDDYS LABORATORIES LTD | PIOGLITAZONE HYDROCHLORIDE |
| 16682 | I | II | 7/3/2003 | SUN PHARMACEUTICAL INDUSTRIES LTD | PIOGLITAZONE HYDROCHLORIDE USP |
| 16684 | A | II | 7/8/2003 | USV PRIVATE LTD | PIOGLITAZONE HYDROCHLORIDE |
| 16688 | A | II | 7/8/2003 | TEVA PHARMACEUTICAL INDUSTRIES LTD | PIOGLITAZONE 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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
