Package 68071-3833-8

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3833-8
Digits Only 6807138338
Product NDC 68071-3833
Product ID 68071-3833_331560b5-d8a7-18ca-e063-6294a90a19f9
Description

180 TABLET, FILM COATED in 1 BOTTLE (68071-3833-8)

Marketing

Marketing Status
Marketed Since 2025-04-18
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": "331560b5-d8a7-18ca-e063-6294a90a19f9", "openfda": {"upc": ["0368071383386"], "unii": ["786Z46389E"], "rxcui": ["861010"], "spl_set_id": ["33155746-c2ef-12f4-e063-6294a90a039c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (68071-3833-8)", "package_ndc": "68071-3833-8", "marketing_start_date": "20250418"}], "brand_name": "Metformin Hydrochloride", "product_id": "68071-3833_331560b5-d8a7-18ca-e063-6294a90a19f9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "68071-3833", "generic_name": "Metformin Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "850 mg/1"}], "application_number": "ANDA209882", "marketing_category": "ANDA", "marketing_start_date": "20210517", "listing_expiration_date": "20261231"}