Package 0615-8577-39
Brand: metformin hydrochloride
Generic: metformin hydrochloridePackage Facts
Identity
Package NDC
0615-8577-39
Digits Only
0615857739
Product NDC
0615-8577
Description
30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8577-39)
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": "27ec7057-a880-4145-a136-0dfb836ebc7d", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004", "861010"], "spl_set_id": ["0448c618-2f0d-4ed3-866f-74b413cf902d"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8577-39)", "package_ndc": "0615-8577-39", "marketing_start_date": "20250418"}], "brand_name": "Metformin Hydrochloride", "product_id": "0615-8577_27ec7057-a880-4145-a136-0dfb836ebc7d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "0615-8577", "generic_name": "Metformin Hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "850 mg/1"}], "application_number": "ANDA077095", "marketing_category": "ANDA", "marketing_start_date": "20240329", "listing_expiration_date": "20261231"}