Package 69367-181-01

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69367-181-01
Digits Only 6936718101
Product NDC 69367-181
Product ID 69367-181_fef0f898-a921-462b-9625-626d0e52d8f5
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-181-01)

Marketing

Marketing Status
Marketed Since 2017-11-21
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": "fef0f898-a921-462b-9625-626d0e52d8f5", "openfda": {"upc": ["0369367180016", "0369367181013", "0369367182010"], "unii": ["786Z46389E"], "rxcui": ["861004", "861007", "861010"], "spl_set_id": ["836f3647-bfef-40d1-b475-c0d240241a67"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-181-01)", "package_ndc": "69367-181-01", "marketing_start_date": "20171121"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-181-05)", "package_ndc": "69367-181-05", "marketing_start_date": "20171121"}], "brand_name": "Metformin Hydrochloride", "product_id": "69367-181_fef0f898-a921-462b-9625-626d0e52d8f5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "69367-181", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "850 mg/1"}], "application_number": "ANDA203769", "marketing_category": "ANDA", "marketing_start_date": "20171121", "listing_expiration_date": "20261231"}