trihexyphenidyl hydrochloride

Generic: trihexyphenidyl hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trihexyphenidyl hydrochloride
Generic Name trihexyphenidyl hydrochloride
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trihexyphenidyl hydrochloride 5 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2409
Product ID 70518-2409_4a17b684-8b80-215c-e063-6394a90a6e19
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040254
Listing Expiration 2027-12-31
Marketing Start 2019-11-08

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182409
Hyphenated Format 70518-2409

Supplemental Identifiers

RxCUI
905283
UNII
AO61G82577

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name trihexyphenidyl hydrochloride (source: ndc)
Generic Name trihexyphenidyl hydrochloride (source: ndc)
Application Number ANDA040254 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 POUCH in 1 BOX (70518-2409-2) / 1 TABLET in 1 POUCH (70518-2409-3)
source: ndc

Packages (1)

70518-2409-2 100 POUCH in 1 BOX (70518-2409-2) / 1 TABLET in 1 POUCH (70518-2409-3)

Ingredients (1)

trihexyphenidyl hydrochloride (5 mg/1)

Linked Drug Pages (1)

TRIHEXYPHENIDYL HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a17b684-8b80-215c-e063-6394a90a6e19", "openfda": {"unii": ["AO61G82577"], "rxcui": ["905283"], "spl_set_id": ["c25ea809-5bdf-4917-97f1-610059fbd0b7"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2409-2)  / 1 TABLET in 1 POUCH (70518-2409-3)", "package_ndc": "70518-2409-2", "marketing_start_date": "20210511"}], "brand_name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "product_id": "70518-2409_4a17b684-8b80-215c-e063-6394a90a6e19", "dosage_form": "TABLET", "product_ndc": "70518-2409", "generic_name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRIHEXYPHENIDYL HYDROCHLORIDE", "active_ingredients": [{"name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA040254", "marketing_category": "ANDA", "marketing_start_date": "20191108", "listing_expiration_date": "20271231"}