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Trihexyphenidyl Hydrochloride - 49349-522-02 - (Trihexyphenidyl Hydrochloride)

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Drug Information of Trihexyphenidyl Hydrochloride

Product NDC: 49349-522
Proprietary Name: Trihexyphenidyl Hydrochloride
Non Proprietary Name: Trihexyphenidyl Hydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   Trihexyphenidyl Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Trihexyphenidyl Hydrochloride

Product NDC: 49349-522
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040337
Marketing Category: ANDA
Start Marketing Date: 20110920

Package Information of Trihexyphenidyl Hydrochloride

Package NDC: 49349-522-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-522-02)

NDC Information of Trihexyphenidyl Hydrochloride

NDC Code 49349-522-02
Proprietary Name Trihexyphenidyl Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (49349-522-02)
Product NDC 49349-522
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trihexyphenidyl Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110920
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name TRIHEXYPHENIDYL HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Trihexyphenidyl Hydrochloride


General Information