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Trihexyphenidyl Hydrochloride - 16571-160-10 - (Trihexyphenidyl Hydrochloride)

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Drug Information of Trihexyphenidyl Hydrochloride

Product NDC: 16571-160
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: 16571-160
Labeler Name: Pack Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091630
Marketing Category: ANDA
Start Marketing Date: 20101117

Package Information of Trihexyphenidyl Hydrochloride

Package NDC: 16571-160-10
Package Description: 100 TABLET in 1 BOTTLE (16571-160-10)

NDC Information of Trihexyphenidyl Hydrochloride

NDC Code 16571-160-10
Proprietary Name Trihexyphenidyl Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (16571-160-10)
Product NDC 16571-160
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trihexyphenidyl Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101117
Marketing Category Name ANDA
Labeler Name Pack Pharmaceuticals, LLC
Substance Name TRIHEXYPHENIDYL HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Trihexyphenidyl Hydrochloride


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