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Pseudoephedrine - 10267-1004-8 - (Pseudoephedrine Hydrochloride)

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Drug Information of Pseudoephedrine

Product NDC: 10267-1004
Proprietary Name: Pseudoephedrine
Non Proprietary Name: Pseudoephedrine Hydrochloride
Active Ingredient(s): 30    mg/1 & nbsp;   Pseudoephedrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pseudoephedrine

Product NDC: 10267-1004
Labeler Name: Contract Pharmacal Corp
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20010621

Package Information of Pseudoephedrine

Package NDC: 10267-1004-8
Package Description: 24 TABLET in 1 BOTTLE (10267-1004-8)

NDC Information of Pseudoephedrine

NDC Code 10267-1004-8
Proprietary Name Pseudoephedrine
Package Description 24 TABLET in 1 BOTTLE (10267-1004-8)
Product NDC 10267-1004
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Pseudoephedrine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010621
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Contract Pharmacal Corp
Substance Name PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Pseudoephedrine


General Information