Package 0378-7186-05

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0378-7186-05
Digits Only 0378718605
Product NDC 0378-7186
Product ID 0378-7186_d1f3ad9f-8f0a-487f-9aad-1b77afe5a03e
Description

500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7186-05)

Marketing

Marketing Status
Marketed Since 2010-06-03
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": "d1f3ad9f-8f0a-487f-9aad-1b77afe5a03e", "openfda": {"upc": ["0303787187057", "0303787185053", "0303787186050"], "unii": ["786Z46389E"], "rxcui": ["861004", "861007", "861010"], "spl_set_id": ["4f70f907-08d5-4c2e-a4be-32c6124faa7b"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7186-05)", "package_ndc": "0378-7186-05", "marketing_start_date": "20100603"}], "brand_name": "Metformin Hydrochloride", "product_id": "0378-7186_d1f3ad9f-8f0a-487f-9aad-1b77afe5a03e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "0378-7186", "generic_name": "metformin hydrochloride", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "850 mg/1"}], "application_number": "ANDA075973", "marketing_category": "ANDA", "marketing_start_date": "20100603", "listing_expiration_date": "20261231"}