Trihexyphenidyl Hydrochloride
TRIHEXYPHENIDYL HYDROCHLORIDE TABLETS, USP
Approved
Approval ID
55790126-5489-4c44-947b-5ac9850b9220
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 12, 2016
Manufacturers
FDA
Richmond Pharmaceuticals, Inc.
DUNS: 043569607
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
trihexyphenidyl hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54738-554
Application NumberANDA040254
Product Classification
M
Marketing Category
C73584
G
Generic Name
trihexyphenidyl hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateAugust 19, 2016
FDA Product Classification
INGREDIENTS (4)
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
TRIHEXYPHENIDYL HYDROCHLORIDEActive
Quantity: 2 mg in 1 1
Code: AO61G82577
Classification: ACTIB
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
trihexyphenidyl hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54738-555
Application NumberANDA040254
Product Classification
M
Marketing Category
C73584
G
Generic Name
trihexyphenidyl hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateAugust 19, 2016
FDA Product Classification
INGREDIENTS (4)
TRIHEXYPHENIDYL HYDROCHLORIDEActive
Quantity: 5 mg in 1 1
Code: AO61G82577
Classification: ACTIB
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT