Package 60760-523-60
Brand: metformin hydrochloride
Generic: metformin hydrochloridePackage Facts
Identity
Package NDC
60760-523-60
Digits Only
6076052360
Product NDC
60760-523
Description
60 TABLET in 1 BOTTLE, PLASTIC (60760-523-60)
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": "ded43b3e-9705-4219-e053-2a95a90a73f2", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["d7103922-2007-1eb4-e053-2995a90aad4e"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (60760-523-60)", "package_ndc": "60760-523-60", "marketing_start_date": "20211228"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "60760-523_ded43b3e-9705-4219-e053-2a95a90a73f2", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "60760-523", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA203769", "marketing_category": "ANDA", "marketing_start_date": "20211228", "listing_expiration_date": "20261231"}