Suphedrine - 11822-0112-2 - (Pseudoephedrine HCl)

Alphabetical Index


Drug Information of Suphedrine

Product NDC: 11822-0112
Proprietary Name: Suphedrine
Non Proprietary Name: Pseudoephedrine HCl
Active Ingredient(s): 30    mg/1 & nbsp;   Pseudoephedrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Suphedrine

Product NDC: 11822-0112
Labeler Name: Rite Aid
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19810825

Package Information of Suphedrine

Package NDC: 11822-0112-2
Package Description: 1 BLISTER PACK in 1 CARTON (11822-0112-2) > 48 TABLET in 1 BLISTER PACK

NDC Information of Suphedrine

NDC Code 11822-0112-2
Proprietary Name Suphedrine
Package Description 1 BLISTER PACK in 1 CARTON (11822-0112-2) > 48 TABLET in 1 BLISTER PACK
Product NDC 11822-0112
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Pseudoephedrine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19810825
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Rite Aid
Substance Name PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Suphedrine


General Information