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Pseudoephedrine Hydrochloride - 63868-143-10 - (Pseudoephedrine Hydrochloride)

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Drug Information of Pseudoephedrine Hydrochloride

Product NDC: 63868-143
Proprietary Name: Pseudoephedrine Hydrochloride
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 Pseudoephedrine Hydrochloride

Product NDC: 63868-143
Labeler Name: Chain Drug Marketing Association Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077442
Marketing Category: ANDA
Start Marketing Date: 20060428

Package Information of Pseudoephedrine Hydrochloride

Package NDC: 63868-143-10
Package Description: 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (63868-143-10)

NDC Information of Pseudoephedrine Hydrochloride

NDC Code 63868-143-10
Proprietary Name Pseudoephedrine Hydrochloride
Package Description 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (63868-143-10)
Product NDC 63868-143
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 20060428
Marketing Category Name ANDA
Labeler Name Chain Drug Marketing Association Inc.
Substance Name PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Pseudoephedrine Hydrochloride


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