Home > National Drug Code (NDC) > Suphedrine PE

Suphedrine PE - 11822-0502-8 - (Acetaminophen and Phenylephrine HCl)

Alphabetical Index


Drug Information of Suphedrine PE

Product NDC: 11822-0502
Proprietary Name: Suphedrine PE
Non Proprietary Name: Acetaminophen and Phenylephrine HCl
Active Ingredient(s): 325; 5    mg/1; mg/1 & nbsp;   Acetaminophen and Phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Suphedrine PE

Product NDC: 11822-0502
Labeler Name: Rite Aid
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20050623

Package Information of Suphedrine PE

Package NDC: 11822-0502-8
Package Description: 1 BLISTER PACK in 1 CARTON (11822-0502-8) > 24 TABLET in 1 BLISTER PACK

NDC Information of Suphedrine PE

NDC Code 11822-0502-8
Proprietary Name Suphedrine PE
Package Description 1 BLISTER PACK in 1 CARTON (11822-0502-8) > 24 TABLET in 1 BLISTER PACK
Product NDC 11822-0502
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen and Phenylephrine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050623
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Rite Aid
Substance Name ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Suphedrine PE


General Information