Package 33342-378-10

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 33342-378-10
Digits Only 3334237810
Product NDC 33342-378
Product ID 33342-378_2737f784-07ad-4e5a-862f-beaea31d005e
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-378-10)

Marketing

Marketing Status
Marketed Since 2024-03-13
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": "2737f784-07ad-4e5a-862f-beaea31d005e", "openfda": {"unii": ["786Z46389E"], "rxcui": ["1807888"], "spl_set_id": ["2737f784-07ad-4e5a-862f-beaea31d005e"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-378-10)", "package_ndc": "33342-378-10", "marketing_start_date": "20240313"}], "brand_name": "Metformin Hydrochloride", "product_id": "33342-378_2737f784-07ad-4e5a-862f-beaea31d005e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "33342-378", "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": "1000 mg/1"}], "application_number": "ANDA211163", "marketing_category": "ANDA", "marketing_start_date": "20240313", "listing_expiration_date": "20261231"}