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Promethazine hydrochloride and phenylephrine hydrochloride - 0472-1628-16 - (Promethazine hydrochloride and phenylephrine hydrochloride)

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Drug Information of Promethazine hydrochloride and phenylephrine hydrochloride

Product NDC: 0472-1628
Proprietary Name: Promethazine hydrochloride and phenylephrine hydrochloride
Non Proprietary Name: Promethazine hydrochloride and phenylephrine hydrochloride
Active Ingredient(s): 5; 6.25    mg/5mL; mg/5mL & nbsp;   Promethazine hydrochloride and phenylephrine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of Promethazine hydrochloride and phenylephrine hydrochloride

Product NDC: 0472-1628
Labeler Name: Actavis Mid Atlantic LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088761
Marketing Category: ANDA
Start Marketing Date: 20111219

Package Information of Promethazine hydrochloride and phenylephrine hydrochloride

Package NDC: 0472-1628-16
Package Description: 473 mL in 1 BOTTLE (0472-1628-16)

NDC Information of Promethazine hydrochloride and phenylephrine hydrochloride

NDC Code 0472-1628-16
Proprietary Name Promethazine hydrochloride and phenylephrine hydrochloride
Package Description 473 mL in 1 BOTTLE (0472-1628-16)
Product NDC 0472-1628
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Promethazine hydrochloride and phenylephrine hydrochloride
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20111219
Marketing Category Name ANDA
Labeler Name Actavis Mid Atlantic LLC
Substance Name PHENYLEPHRINE HYDROCHLORIDE; PROMETHAZINE HYDROCHLORIDE
Strength Number 5; 6.25
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Promethazine hydrochloride and phenylephrine hydrochloride


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