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Trihexyphenidyl Hydrochloride - 0143-1764-10 - (Trihexyphenidyl Hydrochloride)

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Drug Information of Trihexyphenidyl Hydrochloride

Product NDC: 0143-1764
Proprietary Name: Trihexyphenidyl Hydrochloride
Non Proprietary Name: Trihexyphenidyl Hydrochloride
Active Ingredient(s): 2    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: 0143-1764
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040337
Marketing Category: ANDA
Start Marketing Date: 20000216

Package Information of Trihexyphenidyl Hydrochloride

Package NDC: 0143-1764-10
Package Description: 1000 TABLET in 1 BOTTLE (0143-1764-10)

NDC Information of Trihexyphenidyl Hydrochloride

NDC Code 0143-1764-10
Proprietary Name Trihexyphenidyl Hydrochloride
Package Description 1000 TABLET in 1 BOTTLE (0143-1764-10)
Product NDC 0143-1764
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trihexyphenidyl Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000216
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
Substance Name TRIHEXYPHENIDYL HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Trihexyphenidyl Hydrochloride


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