Package 60687-162-01

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-162-01
Digits Only 6068716201
Product NDC 60687-162
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-162-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-162-11)

Marketing

Marketing Status
Marketed Since 2015-10-15
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": "23a82431-7877-94b5-e063-6394a90af9db", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004", "861007", "861010"], "spl_set_id": ["dd54d30b-9390-4e5a-bf62-fbf18b91e4cd"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-162-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-162-11)", "package_ndc": "60687-162-01", "marketing_start_date": "20151015"}], "brand_name": "Metformin Hydrochloride", "product_id": "60687-162_23a82431-7877-94b5-e063-6394a90af9db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "60687-162", "generic_name": "Metformin Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA203686", "marketing_category": "ANDA", "marketing_start_date": "20151015", "listing_expiration_date": "20261231"}