Package 73352-119-60

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 73352-119-60
Digits Only 7335211960
Product NDC 73352-119
Product ID 73352-119_4008fdd6-a9b7-b299-e063-6394a90afdfd
Description

60 TABLET in 1 BOTTLE (73352-119-60)

Marketing

Marketing Status
Marketed Since 2025-07-14
Brand dicyclomine hydrochloride
Generic dicyclomine hydrochloride
Sample Package No

Linked Drug Pages (1)

Dicyclomine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4008fdd6-a9b7-b299-e063-6394a90afdfd", "openfda": {"upc": ["0373352119608"], "unii": ["CQ903KQA31"], "rxcui": ["2719470"], "spl_set_id": ["56282794-5874-4220-b25c-cea4b17d19aa"], "manufacturer_name": ["Trifluent Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (73352-119-60)", "package_ndc": "73352-119-60", "marketing_start_date": "20250714"}], "brand_name": "Dicyclomine hydrochloride", "product_id": "73352-119_4008fdd6-a9b7-b299-e063-6394a90afdfd", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "73352-119", "generic_name": "Dicyclomine hydrochloride", "labeler_name": "Trifluent Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA216736", "marketing_category": "ANDA", "marketing_start_date": "20250714", "listing_expiration_date": "20261231"}