Drug Master Files for: CHLORPROMAZINE
✉ Email this page to a colleague
CHLORPROMAZINE Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 1516 | A | II | 4/23/1970 | SANOFI CHIMIE | CHLORPROMAZINE HYDROCHLORIDE |
| 1616 | I | II | 7/2/1970 | DOLDER AND CO LTD | CHLORPROMAZINE HCL |
| 1730 | I | II | 5/28/1971 | TARO VIT CHEMICAL INDS | CHLORPROMAZINE HCL |
| 1741 | I | II | 6/14/1971 | TARO VIT CHEMICAL INDS | CHLORPROMAZINE HCL |
| 1751 | I | II | 6/29/1971 | DELMAR CHEMICALS INC | CHLORPROMAZINE HCL |
| 1779 | I | II | 8/17/1971 | PCR INC | CHLORPROMAZINE HCL |
| 2104 | I | II | 5/16/1973 | PHENCHEM INDUSTRIES LTD | CHLORPROMAZINE HYDROCHLORIDE |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
