Package 33342-239-11

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 33342-239-11
Digits Only 3334223911
Product NDC 33342-239
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-239-11)

Marketing

Marketing Status
Marketed Since 2016-12-08
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": "3ce6010c-10dd-4e6f-9517-d71c0489a7c5", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975", "860981", "861004", "861007", "861010"], "spl_set_id": ["623b3bc6-1b07-4a04-bc7a-7fc695adf063"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-239-11)", "package_ndc": "33342-239-11", "marketing_start_date": "20161208"}], "brand_name": "Metformin hydrochloride", "product_id": "33342-239_3ce6010c-10dd-4e6f-9517-d71c0489a7c5", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "33342-239", "generic_name": "Metformin hydrochloride", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA206955", "marketing_category": "ANDA", "marketing_start_date": "20161208", "listing_expiration_date": "20261231"}