Package 31722-042-47

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 31722-042-47
Digits Only 3172204247
Product NDC 31722-042
Product ID 31722-042_320180cd-22d3-03bc-e063-6394a90ac74d
Description

1 BOTTLE in 1 CARTON (31722-042-47) / 473 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-03-13
Brand metformin hydrochloride
Generic metformin hydrochloride
Sample Package No

Linked Drug Pages (1)

Metformin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "320180cd-22d3-03bc-e063-6394a90ac74d", "openfda": {"upc": ["0331722042475"], "unii": ["786Z46389E"], "rxcui": ["861025"], "spl_set_id": ["7cc02a26-5c22-445b-ad8f-3e7570c143d3"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (31722-042-47)  / 473 mL in 1 BOTTLE", "package_ndc": "31722-042-47", "marketing_start_date": "20250313"}], "brand_name": "Metformin Hydrochloride", "product_id": "31722-042_320180cd-22d3-03bc-e063-6394a90ac74d", "dosage_form": "SOLUTION", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "31722-042", "generic_name": "Metformin Hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/5mL"}], "application_number": "ANDA215008", "marketing_category": "ANDA", "marketing_start_date": "20250313", "listing_expiration_date": "20261231"}