trihexyphenidyl hydrochloride

Generic: trihexyphenidyl hydrochloride

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

Drug Facts

Product Profile

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

trihexyphenidyl hydrochloride 2 mg/1

Manufacturer
Bionpharma Inc.

Identifiers & Regulatory

Product NDC 69452-241
Product ID 69452-241_38f3f3f8-6374-9981-e063-6294a90aa5df
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091630
Marketing Start 2018-12-15
Marketing End 2026-09-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69452241
Hyphenated Format 69452-241

Supplemental Identifiers

RxCUI
905269 905283
UPC
0369452242322 0369452242209 0369452241202 0369452241325
UNII
AO61G82577

Packaging Origin

Original Packager
true

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 ANDA091630 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69452-241-20)
source: ndc

Packages (1)

69452-241-20 100 TABLET in 1 BOTTLE (69452-241-20)

Ingredients (1)

trihexyphenidyl hydrochloride (2 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": "38f3f3f8-6374-9981-e063-6294a90aa5df", "openfda": {"upc": ["0369452242322", "0369452242209", "0369452241202", "0369452241325"], "unii": ["AO61G82577"], "rxcui": ["905269", "905283"], "spl_set_id": ["4d4d473e-4f84-43e7-bb17-49e8dc1e97fd"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69452-241-20)", "package_ndc": "69452-241-20", "marketing_end_date": "20260930", "marketing_start_date": "20181215"}], "brand_name": "Trihexyphenidyl Hydrochloride", "product_id": "69452-241_38f3f3f8-6374-9981-e063-6294a90aa5df", "dosage_form": "TABLET", "product_ndc": "69452-241", "generic_name": "Trihexyphenidyl Hydrochloride", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trihexyphenidyl Hydrochloride", "active_ingredients": [{"name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA091630", "marketing_category": "ANDA", "marketing_end_date": "20260930", "marketing_start_date": "20181215"}