trihexyphenidyl hydrochloride

Generic: trihexyphenidyl hydrochloride

Labeler: natco pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trihexyphenidyl hydrochloride
Generic Name trihexyphenidyl hydrochloride
Labeler natco pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trihexyphenidyl hydrochloride 2 mg/1

Manufacturer
Natco Pharma Limited

Identifiers & Regulatory

Product NDC 63850-0021
Product ID 63850-0021_2b77cfd6-ad8a-4cbf-a22c-eb69e7a8548c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091630
Listing Expiration 2026-12-31
Marketing Start 2010-10-17

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 638500021
Hyphenated Format 63850-0021

Supplemental Identifiers

RxCUI
905269 905283
UPC
0363850002113 0363850002229
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 (63850-0021-1)
  • 250 TABLET in 1 BOTTLE (63850-0021-2)
  • 1000 TABLET in 1 BOTTLE (63850-0021-3)
source: ndc

Packages (3)

63850-0021-1 100 TABLET in 1 BOTTLE (63850-0021-1) 63850-0021-2 250 TABLET in 1 BOTTLE (63850-0021-2) 63850-0021-3 1000 TABLET in 1 BOTTLE (63850-0021-3)

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": "2b77cfd6-ad8a-4cbf-a22c-eb69e7a8548c", "openfda": {"upc": ["0363850002113", "0363850002229"], "unii": ["AO61G82577"], "rxcui": ["905269", "905283"], "spl_set_id": ["b7e4200c-feff-4537-aad1-cf9989fd8c14"], "manufacturer_name": ["Natco Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63850-0021-1)", "package_ndc": "63850-0021-1", "marketing_start_date": "20101017"}, {"sample": false, "description": "250 TABLET in 1 BOTTLE (63850-0021-2)", "package_ndc": "63850-0021-2", "marketing_start_date": "20101017"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (63850-0021-3)", "package_ndc": "63850-0021-3", "marketing_start_date": "20101017"}], "brand_name": "Trihexyphenidyl Hydrochloride", "product_id": "63850-0021_2b77cfd6-ad8a-4cbf-a22c-eb69e7a8548c", "dosage_form": "TABLET", "product_ndc": "63850-0021", "generic_name": "Trihexyphenidyl Hydrochloride", "labeler_name": "Natco Pharma Limited", "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_start_date": "20101017", "listing_expiration_date": "20261231"}