Drug Master Files for: PIPERACILLIN SODIUM
✉ Email this page to a colleague
PIPERACILLIN SODIUM Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
10112 | I | II | 4/30/1980 | LEDERLE LABORATORIES DIV AMERICAN CYANAMID CO | PIPERACILLIN MONOHYDRATE |
10133 | I | II | 2/2/1982 | BRISTOL MYERS SQUIBB CO | PIPERACILLIN MONOHYDRATE |
12829 | I | II | 1/23/1998 | CORDEN PHARMA LATINA SPA | PIPERACILLIN MONOHYDRATE |
16841 | A | II | 9/15/2003 | YUHAN CHEMICAL INC | PIPERACILLIN MONOHYDRATE |
18161 | A | II | 3/11/2005 | SANDOZ INDUSTRIAL PRODUCTS SA | PIPERACILLIN |
18903 | A | II | 10/25/2005 | SANDOZ INDUSTRIAL PRODUCTS SA | PIPERACILLIN SODIUM & TAZOBACTAM SODIUM (8:1), STERILE |
19031 | A | II | 12/14/2005 | PFIZER HEALTHCARE INDIA PVT LTD | PIPERACILLIN |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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