Package 68071-3900-6
Brand: metformin hydrochloride
Generic: metformin hydrochloridePackage Facts
Identity
Package NDC
68071-3900-6
Digits Only
6807139006
Product NDC
68071-3900
Description
60 TABLET in 1 BOTTLE (68071-3900-6)
Marketing
Marketing Status
Brand
metformin hydrochloride
Generic
metformin hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "403341f8-e63d-9610-e063-6294a90a59ed", "openfda": {"upc": ["0368071390063"], "unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["403349a1-ec19-8982-e063-6294a90aa060"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3900-6)", "package_ndc": "68071-3900-6", "marketing_start_date": "20251002"}], "brand_name": "Metformin Hydrochloride", "product_id": "68071-3900_403341f8-e63d-9610-e063-6294a90a59ed", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "68071-3900", "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": "500 mg/1"}], "application_number": "ANDA090564", "marketing_category": "ANDA", "marketing_start_date": "20190626", "listing_expiration_date": "20261231"}