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Sudafed 12 Hour - 50580-670-30 - (Pseudoephedrine hydrochloride)

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Drug Information of Sudafed 12 Hour

Product NDC: 50580-670
Proprietary Name: Sudafed 12 Hour
Non Proprietary Name: Pseudoephedrine hydrochloride
Active Ingredient(s): 120    mg/1 & nbsp;   Pseudoephedrine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Sudafed 12 Hour

Product NDC: 50580-670
Labeler Name: McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA073585
Marketing Category: ANDA
Start Marketing Date: 20080601

Package Information of Sudafed 12 Hour

Package NDC: 50580-670-30
Package Description: 3 CARTON in 1 PACKAGE (50580-670-30) > 1 BLISTER PACK in 1 CARTON (50580-670-10) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Sudafed 12 Hour

NDC Code 50580-670-30
Proprietary Name Sudafed 12 Hour
Package Description 3 CARTON in 1 PACKAGE (50580-670-30) > 1 BLISTER PACK in 1 CARTON (50580-670-10) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 50580-670
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Pseudoephedrine hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080601
Marketing Category Name ANDA
Labeler Name McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Substance Name PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Sudafed 12 Hour


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