Trihexyphenidyl Hydrochloride
Trihexyphenidyl hydrochloride tablets
Approved
Approval ID
7d7683c6-be72-49d5-a76c-d48e5143d0f0
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 6, 2011
Manufacturers
FDA
TYA Pharmaceuticals
DUNS: 938389038
Products 1
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 Code64725-0161
Application NumberANDA091630
Product Classification
M
Marketing Category
C73584
G
Generic Name
Trihexyphenidyl Hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateMay 3, 2011
FDA Product Classification
INGREDIENTS (4)
TRIHEXYPHENIDYL HYDROCHLORIDEActive
Quantity: 5 mg in 1 1
Code: AO61G82577
Classification: ACTIB
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT