Drug Master Files for: phenazopyridine
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phenazopyridine Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
21285 | A | II | 1/28/2008 | POSH CHEMICALS PRIVATE LTD | PHENAZOPYRIDINE HYDROCHLORIDE USP |
21286 | A | II | 1/28/2008 | POSH CHEMICALS PRIVATE LTD | PHENAZOPYRIDINE DC LACTOSE |
21287 | A | II | 1/28/2008 | POSH CHEMICALS PRIVATE LTD | PHENAZOPYRIDINE DC PVP |
2163 | I | II | 10/4/1973 | DELMAR CHEMICALS INC | PHENAZOPYRIDINE HYDROCHLORIDE (BULK POWDER) |
29532 | I | II | 7/3/2015 | WANBURY LTD | PHENAZOPYRIDINE HYDROCHLORIDE USP |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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