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Pseudoephedrine hydrochloride - 51660-204-21 - (Pseudoephedrine hydrochloride)

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Drug Information of Pseudoephedrine hydrochloride

Product NDC: 51660-204
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
Coding System: National Drug Codes(NDC)

Labeler Information of Pseudoephedrine hydrochloride

Product NDC: 51660-204
Labeler Name: Ohm Laboratories Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077442
Marketing Category: ANDA
Start Marketing Date: 20060428

Package Information of Pseudoephedrine hydrochloride

Package NDC: 51660-204-21
Package Description: 20 TABLET, FILM COATED in 1 BLISTER PACK (51660-204-21)

NDC Information of Pseudoephedrine hydrochloride

NDC Code 51660-204-21
Proprietary Name Pseudoephedrine hydrochloride
Package Description 20 TABLET, FILM COATED in 1 BLISTER PACK (51660-204-21)
Product NDC 51660-204
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Pseudoephedrine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060428
Marketing Category Name ANDA
Labeler Name Ohm Laboratories Inc.
Substance Name PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Pseudoephedrine hydrochloride


General Information