trihexyphenidyl hydrochloride
Generic: trihexyphenidyl hydrochloride
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
trihexyphenidyl hydrochloride
Generic Name
trihexyphenidyl hydrochloride
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
trihexyphenidyl hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-1657
Product ID
70518-1657_494a509a-024c-be2e-e063-6294a90a9b34
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA084364
Listing Expiration
2027-12-31
Marketing Start
2018-11-09
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705181657
Hyphenated Format
70518-1657
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 30 TABLET in 1 BLISTER PACK (70518-1657-0)
- 100 POUCH in 1 BOX (70518-1657-1) / 1 TABLET in 1 POUCH (70518-1657-2)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "494a509a-024c-be2e-e063-6294a90a9b34", "openfda": {"unii": ["AO61G82577"], "rxcui": ["905283"], "spl_set_id": ["3e71b957-9495-4583-8f00-99eac715ff85"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-1657-0)", "package_ndc": "70518-1657-0", "marketing_start_date": "20181109"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-1657-1) / 1 TABLET in 1 POUCH (70518-1657-2)", "package_ndc": "70518-1657-1", "marketing_start_date": "20190123"}], "brand_name": "Trihexyphenidyl Hydrochloride", "product_id": "70518-1657_494a509a-024c-be2e-e063-6294a90a9b34", "dosage_form": "TABLET", "product_ndc": "70518-1657", "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": "20181109", "listing_expiration_date": "20271231"}