Drug Master Files for: L-GLUTAMINE
✉ Email this page to a colleague
L-GLUTAMINE Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
10565 | A | II | 11/12/1993 | SAFC BIOSCIENCES INC | EX-CELL 300 (MBS) W/L-GLUTAMINE, HEPES, NAHC03, GALACTOSE W/O PHENOL RED (CAT. NO. 14035) |
10654 | I | II | 12/28/1993 | KATAYAMA SEIYAKUSYO CO LTD | GLYCL-L-GLUTAMINE |
10884 | I | II | 4/21/1994 | AJINOMOTO CO INC | GLYCYL-L-GLUTAMINE HYDRATE |
11013 | I | II | 8/2/1994 | JRH BIOSCIENCES | RPMI 1640 MEDIUM, W/O L-GLUTAMINE AND W/O PHENOL RED (PROD. NO. 52773) |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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