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Sunmark Nasal Decongestant - 49348-024-04 - (Pseudoephedrine HCl)

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Drug Information of Sunmark Nasal Decongestant

Product NDC: 49348-024
Proprietary Name: Sunmark Nasal Decongestant
Non Proprietary Name: Pseudoephedrine HCl
Active Ingredient(s): 30    mg/1 & nbsp;   Pseudoephedrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Sunmark Nasal Decongestant

Product NDC: 49348-024
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20030815

Package Information of Sunmark Nasal Decongestant

Package NDC: 49348-024-04
Package Description: 1 BLISTER PACK in 1 CARTON (49348-024-04) > 24 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Sunmark Nasal Decongestant

NDC Code 49348-024-04
Proprietary Name Sunmark Nasal Decongestant
Package Description 1 BLISTER PACK in 1 CARTON (49348-024-04) > 24 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 49348-024
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Pseudoephedrine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030815
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson
Substance Name PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Sunmark Nasal Decongestant


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