trihexyphenidyl hydrochloride

Generic: trihexyphenidyl hydrochloride

Labeler: akorn
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trihexyphenidyl hydrochloride
Generic Name trihexyphenidyl hydrochloride
Labeler akorn
Dosage Form SYRUP
Routes
ORAL
Active Ingredients

trihexyphenidyl hydrochloride 2 mg/5mL

Manufacturer
Akorn

Identifiers & Regulatory

Product NDC 61748-054
Product ID 61748-054_3a17b358-46b6-4e74-9788-ccb8acf9ca8f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040251
Listing Expiration 2026-12-31
Marketing Start 2001-03-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 61748054
Hyphenated Format 61748-054

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 ANDA040251 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/5mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE, PLASTIC (61748-054-16)
source: ndc

Packages (1)

Ingredients (1)

trihexyphenidyl hydrochloride (2 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a17b358-46b6-4e74-9788-ccb8acf9ca8f", "openfda": {"unii": ["AO61G82577"], "rxcui": ["905273"], "spl_set_id": ["294cd88d-d9e8-4938-b4be-c3adc4a35de0"], "manufacturer_name": ["Akorn"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (61748-054-16)", "package_ndc": "61748-054-16", "marketing_start_date": "20010301"}], "brand_name": "Trihexyphenidyl Hydrochloride", "product_id": "61748-054_3a17b358-46b6-4e74-9788-ccb8acf9ca8f", "dosage_form": "SYRUP", "product_ndc": "61748-054", "generic_name": "Trihexyphenidyl Hydrochloride", "labeler_name": "Akorn", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trihexyphenidyl Hydrochloride", "active_ingredients": [{"name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "strength": "2 mg/5mL"}], "application_number": "ANDA040251", "marketing_category": "ANDA", "marketing_start_date": "20010301", "listing_expiration_date": "20261231"}