Package 70518-2305-4

Brand: metronidazole

Generic: metronidazole
NDC Package

Package Facts

Identity

Package NDC 70518-2305-4
Digits Only 7051823054
Product NDC 70518-2305
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2305-4)

Marketing

Marketing Status
Marketed Since 2025-09-13
Brand metronidazole
Generic metronidazole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49f24039-2b5d-6462-e063-6294a90a3711", "openfda": {"nui": ["N0000175435", "M0014907"], "unii": ["140QMO216E"], "rxcui": ["311681"], "spl_set_id": ["2f7d84d4-1085-4243-be88-442eecb85205"], "pharm_class_cs": ["Nitroimidazoles [CS]"], "pharm_class_epc": ["Nitroimidazole Antimicrobial [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2305-4)", "package_ndc": "70518-2305-4", "marketing_start_date": "20250913"}], "brand_name": "Metronidazole", "product_id": "70518-2305_49f24039-2b5d-6462-e063-6294a90a3711", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Nitroimidazole Antimicrobial [EPC]", "Nitroimidazoles [CS]"], "product_ndc": "70518-2305", "generic_name": "Metronidazole", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metronidazole", "active_ingredients": [{"name": "METRONIDAZOLE", "strength": "500 mg/1"}], "application_number": "ANDA203458", "marketing_category": "ANDA", "marketing_start_date": "20190909", "listing_expiration_date": "20271231"}