trihexyphenidyl hydrochloride

Generic: trihexyphenidyl hydrochloride

Labeler: pai holdings, llc dba pai pharma
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trihexyphenidyl hydrochloride
Generic Name trihexyphenidyl hydrochloride
Labeler pai holdings, llc dba pai pharma
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

trihexyphenidyl hydrochloride 2 mg/5mL

Manufacturer
PAI Holdings, LLC dba PAI Pharma

Identifiers & Regulatory

Product NDC 0121-0658
Product ID 0121-0658_e3815d2f-f3ee-4cd6-8a2d-518c74787152
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040177
Listing Expiration 2026-12-31
Marketing Start 1997-05-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01210658
Hyphenated Format 0121-0658

Supplemental Identifiers

RxCUI
905273
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 ANDA040177 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/5mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (0121-0658-16)
source: ndc

Packages (1)

0121-0658-16 473 mL in 1 BOTTLE (0121-0658-16)

Ingredients (1)

trihexyphenidyl hydrochloride (2 mg/5mL)

Linked Drug Pages (1)

Trihexyphenidyl Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e3815d2f-f3ee-4cd6-8a2d-518c74787152", "openfda": {"unii": ["AO61G82577"], "rxcui": ["905273"], "spl_set_id": ["9036c9f0-6d2d-4d0f-a20e-e36f9be228f7"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (0121-0658-16)", "package_ndc": "0121-0658-16", "marketing_start_date": "19970515"}], "brand_name": "Trihexyphenidyl Hydrochloride", "product_id": "0121-0658_e3815d2f-f3ee-4cd6-8a2d-518c74787152", "dosage_form": "SOLUTION", "product_ndc": "0121-0658", "generic_name": "Trihexyphenidyl Hydrochloride", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trihexyphenidyl Hydrochloride", "active_ingredients": [{"name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "strength": "2 mg/5mL"}], "application_number": "ANDA040177", "marketing_category": "ANDA", "marketing_start_date": "19970515", "listing_expiration_date": "20261231"}