Drug Master Files for: VERAPAMIL HYDROCHLORIDE
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VERAPAMIL HYDROCHLORIDE Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 16605 | A | II | 5/26/2003 | PIRAMAL ENTERPRISES LTD | VERAPAMIL HYDROCHLORIDE |
| 18523 | I | II | 7/17/2005 | DIVIS LABORATORIES LTD | VERAPAMIL HYDROCHLORIDE USP |
| 32293 | A | II | 12/22/2017 | MYLAN LABORATORIES LTD | VERAPAMIL HYDROCHLORIDE USP |
| 4802 | A | II | 1/24/1983 | RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA | VERAPAMIL HYDROCHLORIDE |
| 4817 | I | II | 2/22/1983 | OMNICHEM NV | VERAPAMIL HCL |
| 4910 | I | II | 3/31/1983 | ABBOTT LABORATORIES | VERAPAMIL AS MNFG IN N.CHICAGO, ILLINOIS |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
