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Pseudoephedrine Hydrochloride - 57344-035-02 - (PSEUDOEPHEDRINE HYDROCHLORIDE)

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Drug Information of Pseudoephedrine Hydrochloride

Product NDC: 57344-035
Proprietary Name: Pseudoephedrine Hydrochloride
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 Pseudoephedrine Hydrochloride

Product NDC: 57344-035
Labeler Name: AAA Pharmaceutical, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121222

Package Information of Pseudoephedrine Hydrochloride

Package NDC: 57344-035-02
Package Description: 1 BLISTER PACK in 1 CARTON (57344-035-02) > 24 TABLET, COATED in 1 BLISTER PACK

NDC Information of Pseudoephedrine Hydrochloride

NDC Code 57344-035-02
Proprietary Name Pseudoephedrine Hydrochloride
Package Description 1 BLISTER PACK in 1 CARTON (57344-035-02) > 24 TABLET, COATED in 1 BLISTER PACK
Product NDC 57344-035
Product Type Name HUMAN OTC DRUG
Non Proprietary Name PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20121222
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name AAA Pharmaceutical, Inc.
Substance Name PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Pseudoephedrine Hydrochloride


General Information