Package 72336-095-30

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72336-095-30
Digits Only 7233609530
Product NDC 72336-095
Product ID 72336-095_2cda4edb-3ee7-0035-e063-6294a90a7800
Description

30 TABLET in 1 BOTTLE (72336-095-30)

Marketing

Marketing Status
Marketed Since 2025-01-23
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": "2cda4edb-3ee7-0035-e063-6294a90a7800", "openfda": {"upc": ["0372336064309", "0372336095303"], "unii": ["786Z46389E"], "rxcui": ["861021", "2703582"], "spl_set_id": ["a2385bcd-0943-4411-8658-c22b50360385"], "manufacturer_name": ["Lifsa Drugs, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72336-095-30)", "package_ndc": "72336-095-30", "marketing_start_date": "20250123"}], "brand_name": "Metformin Hydrochloride", "product_id": "72336-095_2cda4edb-3ee7-0035-e063-6294a90a7800", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72336-095", "generic_name": "Metformin Hydrochloride", "labeler_name": "Lifsa Drugs, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA075972", "marketing_category": "ANDA", "marketing_start_date": "20020124", "listing_expiration_date": "20261231"}