Generated: December 15, 2017
DrugPatentWatch Database Preview
Drug Master Files for: cephalexin
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|1820||I||II||11/10/1971||GLAXO LABORATORIES SA||CEPHALEXIN|
|3118||I||II||11/17/1977||SHIONOGI AND CO LTD||KEFLEX R SUSTAINED RELEASE CAPSULES (CEPHALEXIN MONOHYDRATE LILLY)|
|6090||I||II||11/12/1985||ELI LILLY INDUSTRIES INC||CEPHALEXIN HYDROCHLORIDE,BULK|
|9889||I||II||9/21/1992||ELANCO QUIMICA LIMITADA||CEPHALEXIN DISOLVATE|
|13210||A||II||4/30/1998||DSM SINOCHEM PHARMACEUTICALS NETHERLANDS BV||CEPHALEXIN MONOHYDRATE |
|13385||I||II||9/1/1998||LILLY RESEARCH LABORATORIES||CEPHALEXIN MONOHYDRATE|
|13588||A||II||9/1/1998||ANTIBIOTICOS SA||CEPHALEXIN MONOHYDRATE|
| This preview shows a limited data set|
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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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
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