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PROMETHEGAN - 0713-0526-12 - (PROMETHAZINE HYDROCHLORIDE)

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Drug Information of PROMETHEGAN

Product NDC: 0713-0526
Proprietary Name: PROMETHEGAN
Non Proprietary Name: PROMETHAZINE HYDROCHLORIDE
Active Ingredient(s): 25    mg/1 & nbsp;   PROMETHAZINE HYDROCHLORIDE
Administration Route(s): RECTAL
Dosage Form(s): SUPPOSITORY
Coding System: National Drug Codes(NDC)

Labeler Information of PROMETHEGAN

Product NDC: 0713-0526
Labeler Name: GW Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040428
Marketing Category: ANDA
Start Marketing Date: 20020228

Package Information of PROMETHEGAN

Package NDC: 0713-0526-12
Package Description: 12 SUPPOSITORY in 1 BOX (0713-0526-12)

NDC Information of PROMETHEGAN

NDC Code 0713-0526-12
Proprietary Name PROMETHEGAN
Package Description 12 SUPPOSITORY in 1 BOX (0713-0526-12)
Product NDC 0713-0526
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PROMETHAZINE HYDROCHLORIDE
Dosage Form Name SUPPOSITORY
Route Name RECTAL
Start Marketing Date 20020228
Marketing Category Name ANDA
Labeler Name GW Laboratories, Inc.
Substance Name PROMETHAZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of PROMETHEGAN


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