Package 73473-902-01
Brand: dicyclomine hydrochloride
Generic: dicyclomine hydrochloridePackage Facts
Identity
Package NDC
73473-902-01
Digits Only
7347390201
Product NDC
73473-902
Description
100 TABLET in 1 BOTTLE (73473-902-01)
Marketing
Marketing Status
Brand
dicyclomine hydrochloride
Generic
dicyclomine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "98b3a053-2708-460d-9929-d89164cd4a49", "openfda": {"upc": ["0373473902103", "0373473902011"], "unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["d46259e6-5eca-4356-bc18-815104c925cc"], "manufacturer_name": ["Solaris Pharma Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (73473-902-01)", "package_ndc": "73473-902-01", "marketing_start_date": "20250610"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (73473-902-10)", "package_ndc": "73473-902-10", "marketing_start_date": "20250610"}], "brand_name": "DICYCLOMINE HYDROCHLORIDE", "product_id": "73473-902_98b3a053-2708-460d-9929-d89164cd4a49", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "73473-902", "generic_name": "DICYCLOMINE HYDROCHLORIDE", "labeler_name": "Solaris Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DICYCLOMINE HYDROCHLORIDE", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA216760", "marketing_category": "ANDA", "marketing_start_date": "20250610", "listing_expiration_date": "20261231"}