Package 72664-228-90
Brand: metformin hydrochloride
Generic: metformin hydrochloridePackage Facts
Identity
Package NDC
72664-228-90
Digits Only
7266422890
Product NDC
72664-228
Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72664-228-90)
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": "05f10272-9976-b4f6-e063-6294a90a0092", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975", "1807888"], "spl_set_id": ["129ff158-097f-401a-8924-d9258465c1f3"], "manufacturer_name": ["VGYAAN Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72664-228-90)", "package_ndc": "72664-228-90", "marketing_start_date": "20211130"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "72664-228_05f10272-9976-b4f6-e063-6294a90a0092", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72664-228", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "VGYAAN Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA215629", "marketing_category": "ANDA", "marketing_start_date": "20211130", "listing_expiration_date": "20261231"}