Drug Master Files for: NEOMYCIN SULFATE
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NEOMYCIN SULFATE Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
110 | I | II | 5/29/1953 | SB PENICK AND CO | NEOMYCIN SULFATE USP |
124 | I | II | 7/23/1953 | PFIZER INC | NEOMYCIN SULFATE CAPS (THIS D CHANGED TO NDA 9-579) |
13286 | I | II | 9/1/1998 | PENICK CORP | NEOMYCIN SULFATE |
13378 | A | II | 9/1/1998 | PHARMACIA AND UPJOHN CO WHOLLY OWNED SUB PFIZER INC | NEOMYCIN SULFATE USP |
13528 | I | II | 9/1/1998 | APOTHEKERNES LABORATORIUM AS | NEOMYCIN SULFATE |
13609 | I | II | 9/1/1998 | APOTHEKERNES LABORATORIUM AS | NEOMYCIN SULFATE |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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