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PROMETHAZINE DM - 54868-1990-0 - (Dextromethorphan Hydrobromide and Promethazine Hydrochloride)

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Drug Information of PROMETHAZINE DM

Product NDC: 54868-1990
Proprietary Name: PROMETHAZINE DM
Non Proprietary Name: Dextromethorphan Hydrobromide and Promethazine Hydrochloride
Active Ingredient(s): 15; 6.25    mg/5mL; mg/5mL & nbsp;   Dextromethorphan Hydrobromide and Promethazine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of PROMETHAZINE DM

Product NDC: 54868-1990
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040649
Marketing Category: ANDA
Start Marketing Date: 20071004

Package Information of PROMETHAZINE DM

Package NDC: 54868-1990-0
Package Description: 118 mL in 1 BOTTLE (54868-1990-0)

NDC Information of PROMETHAZINE DM

NDC Code 54868-1990-0
Proprietary Name PROMETHAZINE DM
Package Description 118 mL in 1 BOTTLE (54868-1990-0)
Product NDC 54868-1990
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dextromethorphan Hydrobromide and Promethazine Hydrochloride
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20071004
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; PROMETHAZINE HYDROCHLORIDE
Strength Number 15; 6.25
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC],Sigma-1 Agonist [EPC],Uncompetitive NMDA Receptor Antagonists [MoA],Sigma-1 Receptor Agonists [MoA],Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of PROMETHAZINE DM


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