Package 67877-218-38

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67877-218-38
Digits Only 6787721838
Product NDC 67877-218
Product ID 67877-218_4fa6bd66-7f2c-4b63-9809-be460cbc2527
Description

10 BLISTER PACK in 1 CARTON (67877-218-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK (67877-218-33)

Marketing

Marketing Status
Marketed Since 2011-01-31
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": "4fa6bd66-7f2c-4b63-9809-be460cbc2527", "openfda": {"upc": ["0367877221014", "0367877218014", "0367877414904", "0367877413907"], "unii": ["786Z46389E"], "rxcui": ["860975", "860981", "861004", "861007", "861010"], "spl_set_id": ["0ff1ba75-3c86-4baf-a6b1-1bb883839866"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (67877-218-01)", "package_ndc": "67877-218-01", "marketing_start_date": "20110131"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (67877-218-05)", "package_ndc": "67877-218-05", "marketing_start_date": "20110131"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (67877-218-10)", "package_ndc": "67877-218-10", "marketing_start_date": "20110131"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (67877-218-38)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (67877-218-33)", "package_ndc": "67877-218-38", "marketing_start_date": "20110131"}], "brand_name": "Metformin Hydrochloride", "product_id": "67877-218_4fa6bd66-7f2c-4b63-9809-be460cbc2527", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "67877-218", "generic_name": "Metformin Hydrochloride", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "850 mg/1"}], "application_number": "ANDA091184", "marketing_category": "ANDA", "marketing_start_date": "20110131", "listing_expiration_date": "20261231"}