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PROMETHAZINE HYDROCHLORIDE - 0904-5840-61 - (PROMETHAZINE HYDROCHLORIDE)

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Drug Information of PROMETHAZINE HYDROCHLORIDE

Product NDC: 0904-5840
Proprietary Name: PROMETHAZINE HYDROCHLORIDE
Non Proprietary Name: PROMETHAZINE HYDROCHLORIDE
Active Ingredient(s): 25    mg/1 & nbsp;   PROMETHAZINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of PROMETHAZINE HYDROCHLORIDE

Product NDC: 0904-5840
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040712
Marketing Category: ANDA
Start Marketing Date: 20080509

Package Information of PROMETHAZINE HYDROCHLORIDE

Package NDC: 0904-5840-61
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (0904-5840-61)

NDC Information of PROMETHAZINE HYDROCHLORIDE

NDC Code 0904-5840-61
Proprietary Name PROMETHAZINE HYDROCHLORIDE
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (0904-5840-61)
Product NDC 0904-5840
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PROMETHAZINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080509
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name PROMETHAZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of PROMETHAZINE HYDROCHLORIDE


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