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Non-Drowsy Nasal Decongestant - 59779-112-22 - (Pseudoephedrine HCl)

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Drug Information of Non-Drowsy Nasal Decongestant

Product NDC: 59779-112
Proprietary Name: Non-Drowsy Nasal Decongestant
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 Non-Drowsy Nasal Decongestant

Product NDC: 59779-112
Labeler Name: WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19810825

Package Information of Non-Drowsy Nasal Decongestant

Package NDC: 59779-112-22
Package Description: 1 BLISTER PACK in 1 CARTON (59779-112-22) > 48 TABLET in 1 BLISTER PACK

NDC Information of Non-Drowsy Nasal Decongestant

NDC Code 59779-112-22
Proprietary Name Non-Drowsy Nasal Decongestant
Package Description 1 BLISTER PACK in 1 CARTON (59779-112-22) > 48 TABLET in 1 BLISTER PACK
Product NDC 59779-112
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 WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Substance Name PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Non-Drowsy Nasal Decongestant


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