PRIMATENE - 0573-2952-10 - (ephedrine hcl, guaifenesin)

Alphabetical Index


Drug Information of PRIMATENE

Product NDC: 0573-2952
Proprietary Name: PRIMATENE
Non Proprietary Name: ephedrine hcl, guaifenesin
Active Ingredient(s): 12.5; 200    mg/1; mg/1 & nbsp;   ephedrine hcl, guaifenesin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of PRIMATENE

Product NDC: 0573-2952
Labeler Name: Pfizer Consumer Healthcare
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20040106

Package Information of PRIMATENE

Package NDC: 0573-2952-10
Package Description: 2 BLISTER PACK in 1 CARTON (0573-2952-10) > 12 TABLET in 1 BLISTER PACK

NDC Information of PRIMATENE

NDC Code 0573-2952-10
Proprietary Name PRIMATENE
Package Description 2 BLISTER PACK in 1 CARTON (0573-2952-10) > 12 TABLET in 1 BLISTER PACK
Product NDC 0573-2952
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ephedrine hcl, guaifenesin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040106
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Pfizer Consumer Healthcare
Substance Name EPHEDRINE HYDROCHLORIDE; GUAIFENESIN
Strength Number 12.5; 200
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of PRIMATENE


General Information