Package 71093-134-04

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71093-134-04
Digits Only 7109313404
Product NDC 71093-134
Description

100 TABLET in 1 BOTTLE, PLASTIC (71093-134-04)

Marketing

Marketing Status
Marketed Since 2018-01-15
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": "39bb2259-ba80-4602-b468-a2e0d61f48f6", "openfda": {"upc": ["0371093133044", "0371093134041", "0371093132047"], "unii": ["786Z46389E"], "rxcui": ["861004", "861007", "861010"], "spl_set_id": ["e18b60f9-721e-4db6-9f61-d3437e18faf2"], "manufacturer_name": ["ACI Healthcare USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (71093-134-04)", "package_ndc": "71093-134-04", "marketing_start_date": "20180115"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (71093-134-05)", "package_ndc": "71093-134-05", "marketing_start_date": "20180115"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "71093-134_39bb2259-ba80-4602-b468-a2e0d61f48f6", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "71093-134", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "ACI Healthcare USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA203769", "marketing_category": "ANDA", "marketing_start_date": "20180115", "listing_expiration_date": "20261231"}