Drug Master Files for: AMMONIUM LACTATE
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AMMONIUM LACTATE Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
10629 | A | IV | 12/21/1993 | NOF CORP | 1,2-DIMYRISTOL-SN-GLYCERO-3-PHOSPHATIDYL GLYCERO AMMONIUM/SODIUM SALT |
11 | I | II | 3/12/1944 | ROHM AND HAAS CO | HYAMINE X (QUATERNARY AMMONIUM CHLORIDE COMPOUND) |
11075 | I | II | 9/13/1994 | PURAC BIOCHEM BV | AMMONIUM LACTATE, PURASAL NH 70 |
11103 | I | II | 9/8/1994 | WHATMAN | EXPRESS-ION EXCHANGER Q (QUATERNARY AMMONIUM CELLULOSE) |
11463 | A | II | 4/12/1995 | NOF CORP | DIMYRISTOYL PHOSPHATIDYL GLYCEROL AMMONIUM/SODIUM SALT |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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