Drug Master Files for: pilocarpine hydrochloride
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pilocarpine hydrochloride Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
10025 | A | II | 12/28/1992 | ANIDRO DO BRASIL EXTRACOES SA | PILOCARPINE HYDROCHLORIDE USP |
10861 | I | II | 2/28/1994 | PVP SOCIEDADE ANONIMA | PILOCARPINE HYDROCHLORIDE |
11029 | I | II | 8/10/1994 | PVP SOCIEDADE ANONIMA | PILOCARPINE NITRATE |
12388 | A | II | 2/21/1997 | IWAKI SEIYAKU CO LTD | PILOCARPINE HYDROCHLORIDE |
12629 | I | II | 8/15/1997 | VEGEFLORA EXTRACOES DO NORDESTE LTDA | PILOCARPINE USP |
16873 | A | II | 9/25/2003 | SOURCETECH QUIMICA LTDA | PILOCARPINE 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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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