Package 72189-150-30
Brand: metformin hydrochloride
Generic: metformin hydrochloridePackage Facts
Identity
Package NDC
72189-150-30
Digits Only
7218915030
Product NDC
72189-150
Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-150-30)
Marketing
Marketing Status
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": "2c4ea7fa-b789-8bdf-e063-6394a90a3e5a", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["a84cf1a3-3820-cd1b-e053-2995a90acf45"], "manufacturer_name": ["direct rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-150-30)", "package_ndc": "72189-150-30", "marketing_start_date": "20201014"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-150-90)", "package_ndc": "72189-150-90", "marketing_start_date": "20201014"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "72189-150_2c4ea7fa-b789-8bdf-e063-6394a90a3e5a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72189-150", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "direct rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA078321", "marketing_category": "ANDA", "marketing_start_date": "20201014", "listing_expiration_date": "20261231"}