SUDAFED - 50580-545-24 - (Pseudoephedrine Hydrochloride)

Alphabetical Index


Drug Information of SUDAFED

Product NDC: 50580-545
Proprietary Name: SUDAFED
Non Proprietary Name: Pseudoephedrine Hydrochloride
Active Ingredient(s): 30    mg/1 & nbsp;   Pseudoephedrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of SUDAFED

Product NDC: 50580-545
Labeler Name: McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20111001

Package Information of SUDAFED

Package NDC: 50580-545-24
Package Description: 3 BLISTER PACK in 1 CARTON (50580-545-24) > 8 TABLET, COATED in 1 BLISTER PACK

NDC Information of SUDAFED

NDC Code 50580-545-24
Proprietary Name SUDAFED
Package Description 3 BLISTER PACK in 1 CARTON (50580-545-24) > 8 TABLET, COATED in 1 BLISTER PACK
Product NDC 50580-545
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Pseudoephedrine Hydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20111001
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Substance Name PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of SUDAFED


General Information