trihexyphenidyl hydrochloride

Generic: trihexyphenidyl hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trihexyphenidyl hydrochloride
Generic Name trihexyphenidyl hydrochloride
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trihexyphenidyl hydrochloride 5 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-1140
Product ID 70518-1140_485b95c5-2a90-3aa3-e063-6394a90a10d7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA084364
Listing Expiration 2027-12-31
Marketing Start 2018-04-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705181140
Hyphenated Format 70518-1140

Supplemental Identifiers

RxCUI
905283
UNII
AO61G82577

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 ANDA084364 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-1140-0)
source: ndc

Packages (1)

70518-1140-0 30 TABLET in 1 BLISTER PACK (70518-1140-0)

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": "485b95c5-2a90-3aa3-e063-6394a90a10d7", "openfda": {"unii": ["AO61G82577"], "rxcui": ["905283"], "spl_set_id": ["3ed3cdf1-1745-4c6f-bb90-fb7d9471270d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-1140-0)", "package_ndc": "70518-1140-0", "marketing_start_date": "20180426"}], "brand_name": "Trihexyphenidyl Hydrochloride", "product_id": "70518-1140_485b95c5-2a90-3aa3-e063-6394a90a10d7", "dosage_form": "TABLET", "product_ndc": "70518-1140", "generic_name": "Trihexyphenidyl Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trihexyphenidyl Hydrochloride", "active_ingredients": [{"name": "TRIHEXYPHENIDYL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA084364", "marketing_category": "ANDA", "marketing_start_date": "20180426", "listing_expiration_date": "20271231"}