trihexyphenidyl hydrochloride

Generic: trihexyphenidyl hydrochloride

Labeler: novitium pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trihexyphenidyl hydrochloride
Generic Name trihexyphenidyl hydrochloride
Labeler novitium pharma llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trihexyphenidyl hydrochloride 5 mg/1

Manufacturer
Novitium Pharma LLC

Identifiers & Regulatory

Product NDC 70954-211
Product ID 70954-211_83608c13-509d-448b-8559-5f5e8a9a0d75
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040254
Listing Expiration 2026-12-31
Marketing Start 2019-01-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70954211
Hyphenated Format 70954-211

Supplemental Identifiers

RxCUI
905269 905283
UPC
0370954212102 0370954211105
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 ANDA040254 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70954-211-10)
  • 1000 TABLET in 1 BOTTLE (70954-211-20)
source: ndc

Packages (2)

70954-211-10 100 TABLET in 1 BOTTLE (70954-211-10) 70954-211-20 1000 TABLET in 1 BOTTLE (70954-211-20)

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": "83608c13-509d-448b-8559-5f5e8a9a0d75", "openfda": {"upc": ["0370954212102", "0370954211105"], "unii": ["AO61G82577"], "rxcui": ["905269", "905283"], "spl_set_id": ["83608c13-509d-448b-8559-5f5e8a9a0d75"], "manufacturer_name": ["Novitium Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70954-211-10)", "package_ndc": "70954-211-10", "marketing_start_date": "20190128"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (70954-211-20)", "package_ndc": "70954-211-20", "marketing_start_date": "20190128"}], "brand_name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "product_id": "70954-211_83608c13-509d-448b-8559-5f5e8a9a0d75", "dosage_form": "TABLET", "product_ndc": "70954-211", "generic_name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "labeler_name": "Novitium Pharma LLC", "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": "20190128", "listing_expiration_date": "20261231"}