Drug Master Files for: AMPICILLIN SODIUM

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AMPICILLIN SODIUM Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
11450	I	II	4/14/1995	CONSOLIDATED PHARMACEUTICAL GROUP INC	AMPICILLIN TRIHYDRATE BPC
11482	I	II	4/28/1995	CONSOLIDATED PHARMACEUTICAL GROUP INC	AMPICILLIN TRIHYDRATE FOR ORAL SUSPENSION
11484	I	II	4/28/1995	CONSOLIDATED PHARMACEUTICAL GROUP INC	AMPICILLIN TRIHYDRATE CAPSULES
13212	A	II	4/30/1998	SANDOZ INDUSTRIAL PRODUCTS SA	AMPICILLIN ANHYDROUS
13296	I	II	9/1/1998	SMITHKLINE BEECHAM PHARMACEUTICALS	AMPICILLIN TRIHYDRATE
13297	I	II	9/1/1998	SMITHKLINE BEECHAM PHARMACEUTICALS	AMPICILLIN
>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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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