Drug Master Files for: LEVOBUNOLOL HYDROCHLORIDE

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LEVOBUNOLOL HYDROCHLORIDE Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
11519	I	II	5/19/1995	PLAISTOW LTD	LEVOBUNOLOL HYDROCHLORIDE
14195	A	II	6/7/1999	OLON SPA	LEVOBUNOLOL HYDROCHLORIDE
16904	A	II	10/16/2003	PIRAMAL ENTERPRISES LTD	LEVOBUNOLOL HYDROCHLORIDE
5113	I	II	9/15/1983	GOEDECKE AG	LEVOBUNOLOL HYDROCHLORIDE (1-BUNOLOL 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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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

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