Home > National Drug Code (NDC) > Trihexyphenidyl Hydrochloride

Trihexyphenidyl Hydrochloride - 0591-5335-10 - (Trihexyphenidyl Hydrochloride)

Alphabetical Index


Drug Information of Trihexyphenidyl Hydrochloride

Product NDC: 0591-5335
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: 0591-5335
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084363
Marketing Category: ANDA
Start Marketing Date: 19871101

Package Information of Trihexyphenidyl Hydrochloride

Package NDC: 0591-5335-10
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (0591-5335-10)

NDC Information of Trihexyphenidyl Hydrochloride

NDC Code 0591-5335-10
Proprietary Name Trihexyphenidyl Hydrochloride
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (0591-5335-10)
Product NDC 0591-5335
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trihexyphenidyl Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19871101
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
Substance Name TRIHEXYPHENIDYL HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Trihexyphenidyl Hydrochloride


General Information