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PROMETHAZINE HYDROCHLORIDE - 39822-5500-6 - (PROMETHAZINE HYDROCHLORIDE)

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Drug Information of PROMETHAZINE HYDROCHLORIDE

Product NDC: 39822-5500
Proprietary Name: PROMETHAZINE HYDROCHLORIDE
Non Proprietary Name: PROMETHAZINE HYDROCHLORIDE
Active Ingredient(s): 25    mg/mL & nbsp;   PROMETHAZINE HYDROCHLORIDE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of PROMETHAZINE HYDROCHLORIDE

Product NDC: 39822-5500
Labeler Name: X-GEN Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040737
Marketing Category: ANDA
Start Marketing Date: 20110502

Package Information of PROMETHAZINE HYDROCHLORIDE

Package NDC: 39822-5500-6
Package Description: 25 AMPULE in 1 CARTON (39822-5500-6) > 2 mL in 1 AMPULE (39822-5500-5)

NDC Information of PROMETHAZINE HYDROCHLORIDE

NDC Code 39822-5500-6
Proprietary Name PROMETHAZINE HYDROCHLORIDE
Package Description 25 AMPULE in 1 CARTON (39822-5500-6) > 2 mL in 1 AMPULE (39822-5500-5)
Product NDC 39822-5500
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PROMETHAZINE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20110502
Marketing Category Name ANDA
Labeler Name X-GEN Pharmaceuticals, Inc.
Substance Name PROMETHAZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/mL
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of PROMETHAZINE HYDROCHLORIDE


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