Trihexyphenidyl Hydrochloride

Product NDC

70518-0569

11-digit product format

705180569

Labeler code

70518

Product ID

70518-0569_85d46e57-da81-7368-e053-2a91aa0aa876

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Trihexyphenidyl Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA091630

Marketing category

ANDA

Marketing start

2017-06-06

Marketing end

0000-00-00

Substance

TRIHEXYPHENIDYL HYDROCHLORIDE

Active strength

2 mg/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record