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Trihexyphenidyl Hydrochloride - 54738-555-03 - (trihexyphenidyl hydrochloride)

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Drug Information of Trihexyphenidyl Hydrochloride

Product NDC: 54738-555
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: 54738-555
Labeler Name: Richmond Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040254
Marketing Category: ANDA
Start Marketing Date: 19981224

Package Information of Trihexyphenidyl Hydrochloride

Package NDC: 54738-555-03
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (54738-555-03)

NDC Information of Trihexyphenidyl Hydrochloride

NDC Code 54738-555-03
Proprietary Name Trihexyphenidyl Hydrochloride
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (54738-555-03)
Product NDC 54738-555
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name trihexyphenidyl hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19981224
Marketing Category Name ANDA
Labeler Name Richmond Pharmaceuticals, Inc.
Substance Name TRIHEXYPHENIDYL HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Trihexyphenidyl Hydrochloride


General Information