Drug Master Files for: NEOSTIGMINE METHYLSULFATE
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NEOSTIGMINE METHYLSULFATE Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
24760 | A | II | 3/16/2011 | PATHEON AUSTRIA GMBH AND CO KG | NEOSTIGMINE METHYLSULFATE |
28397 | A | II | 7/8/2014 | EMCURE PHARMACEUTICALS LTD | NEOSTIGMINE METHYLSULFATE USP |
29197 | A | II | 3/31/2015 | MSN LABORATORIES PRIVATE LTD | NEOSTIGMINE METHYLSULFATE USP [ROUTE CODE NS] |
30136 | A | II | 12/31/2015 | HARMAN FINOCHEM LTD | NEOSTIGMINE METHYLSULFATE USP |
31003 | A | II | 11/30/2016 | INDOCO REMEDIES LTD | NEOSTIGMINE METHYLSULFATE USP |
31387 | A | II | 3/5/2018 | ENALTEC LABS PRIVATE LTD | NEOSTIGMINE METHYLSULFATE USP |
32153 | A | II | 10/31/2017 | GLAND PHARMA LTD | NEOSTIGMINE METHYLSULFATE |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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