trihexyphenidyl hydrochloride

Generic: trihexyphenidyl hydrochloride

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trihexyphenidyl hydrochloride
Generic Name trihexyphenidyl hydrochloride
Labeler actavis pharma, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trihexyphenidyl hydrochloride 2 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 0591-5335
Product ID 0591-5335_0b42f7c5-1597-46fd-bc35-5f9286d27877
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA084363
Listing Expiration 2026-12-31
Marketing Start 1987-11-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05915335
Hyphenated Format 0591-5335

Supplemental Identifiers

RxCUI
905269 905283
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 ANDA084363 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (0591-5335-01)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (0591-5335-10)
source: ndc

Packages (2)

0591-5335-01 100 TABLET in 1 BOTTLE, PLASTIC (0591-5335-01) 0591-5335-10 1000 TABLET in 1 BOTTLE, PLASTIC (0591-5335-10)

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": "0b42f7c5-1597-46fd-bc35-5f9286d27877", "openfda": {"unii": ["AO61G82577"], "rxcui": ["905269", "905283"], "spl_set_id": ["a44d7803-164d-4a67-9356-581c45de8596"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0591-5335-01)", "package_ndc": "0591-5335-01", "marketing_start_date": "19871101"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0591-5335-10)", "package_ndc": "0591-5335-10", "marketing_start_date": "19871101"}], "brand_name": "Trihexyphenidyl Hydrochloride", "product_id": "0591-5335_0b42f7c5-1597-46fd-bc35-5f9286d27877", "dosage_form": "TABLET", "product_ndc": "0591-5335", "generic_name": "Trihexyphenidyl Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trihexyphenidyl Hydrochloride", "active_ingredients": [{"name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA084363", "marketing_category": "ANDA", "marketing_start_date": "19871101", "listing_expiration_date": "20261231"}