Package 70518-1149-0

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1149-0
Digits Only 7051811490
Product NDC 70518-1149
Product ID 70518-1149_485bbb02-f1fd-569a-e063-6294a90a8ecb
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1149-0)

Marketing

Marketing Status
Marketed Since 2018-05-01
Brand metformin hydrochloride
Generic metformin hydrochloride
Sample Package No

Linked Drug Pages (1)

Metformin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "485bbb02-f1fd-569a-e063-6294a90a8ecb", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["073cf6d9-7142-4d8b-898e-174c62a1f76f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1149-0)", "package_ndc": "70518-1149-0", "marketing_start_date": "20180501"}], "brand_name": "Metformin Hydrochloride", "product_id": "70518-1149_485bbb02-f1fd-569a-e063-6294a90a8ecb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "70518-1149", "generic_name": "Metformin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077095", "marketing_category": "ANDA", "marketing_start_date": "20180501", "listing_expiration_date": "20271231"}