Drug Master Files for: LIDOCAINE HYDROCHLORIDE
✉ Email this page to a colleague
LIDOCAINE HYDROCHLORIDE Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
11338 | A | II | 2/10/1995 | DELTA SYNTHETIC CO LTD | LIDOCAINE HYDROCHLORIDE |
11339 | A | II | 2/10/1995 | DELTA SYNTHETIC CO LTD | LIDOCAINE |
11564 | A | II | 6/5/1995 | ALBEMARLE CORP | LIDOCAINE USP |
13235 | A | II | 9/25/1998 | MOEHS IBERICA SL | LIDOCAINE |
17483 | I | II | 6/21/2004 | GUFIC BIOSCIENCES LTD | LIDOCAINE HYDROCHLORIDE |
18005 | I | II | 1/10/2005 | SYN-TECH CHEM AND PHARM CO LTD | LIDOCAINE USP |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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