Package 72162-2403-2
Brand: metronidazole
Generic: metronidazolePackage Facts
Identity
Package NDC
72162-2403-2
Digits Only
7216224032
Product NDC
72162-2403
Description
14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2403-2)
Marketing
Marketing Status
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": "9e05f3f2-a880-4e10-af96-479bba15d947", "openfda": {"nui": ["N0000175435", "M0014907"], "unii": ["140QMO216E"], "rxcui": ["311681"], "spl_set_id": ["daee5e69-aa86-470b-81b7-3074d27fc847"], "pharm_class_cs": ["Nitroimidazoles [CS]"], "pharm_class_epc": ["Nitroimidazole Antimicrobial [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2403-2)", "package_ndc": "72162-2403-2", "marketing_start_date": "20241008"}], "brand_name": "Metronidazole", "product_id": "72162-2403_9e05f3f2-a880-4e10-af96-479bba15d947", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Nitroimidazole Antimicrobial [EPC]", "Nitroimidazoles [CS]"], "product_ndc": "72162-2403", "generic_name": "Metronidazole", "labeler_name": "Bryant Ranch Prepack", "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": "20140601", "listing_expiration_date": "20261231"}