Package 68180-339-09
Brand: metformin hydrochloride
Generic: metformin hydrochloridePackage Facts
Identity
Package NDC
68180-339-09
Digits Only
6818033909
Product NDC
68180-339
Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-339-09)
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": "2da9ae97-97e8-43fe-b92a-00f3f7c25673", "openfda": {"unii": ["786Z46389E"], "rxcui": ["1807888", "1807915"], "spl_set_id": ["1200ea71-8a9e-4e49-bb77-7d9fe0d84ae7"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-339-09)", "package_ndc": "68180-339-09", "marketing_start_date": "20160201"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "68180-339_2da9ae97-97e8-43fe-b92a-00f3f7c25673", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "68180-339", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA091664", "marketing_category": "ANDA", "marketing_start_date": "20160201", "listing_expiration_date": "20261231"}