Package 51672-4026-1

Brand: ketoconazole

Generic: ketoconazole
NDC Package

Package Facts

Identity

Package NDC 51672-4026-1
Digits Only 5167240261
Product NDC 51672-4026
Description

100 TABLET in 1 BOTTLE (51672-4026-1)

Marketing

Marketing Status
Marketed Since 1999-06-15
Brand ketoconazole
Generic ketoconazole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3dd44662-95fb-0d34-e063-6294a90a5fbc", "openfda": {"nui": ["N0000175487", "M0002083", "N0000182141", "N0000190115", "N0000185503"], "upc": ["0351672402662"], "unii": ["R9400W927I"], "rxcui": ["197853"], "spl_set_id": ["8ca815a8-bccb-4ee2-a042-922373329cae"], "pharm_class_cs": ["Azoles [CS]"], "pharm_class_epc": ["Azole Antifungal [EPC]"], "pharm_class_moa": ["Cytochrome P450 3A4 Inhibitors [MoA]", "Cytochrome P450 3A5 Inhibitors [MoA]", "P-Glycoprotein Inhibitors [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BOX (51672-4026-0)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "51672-4026-0", "marketing_start_date": "19990615"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (51672-4026-1)", "package_ndc": "51672-4026-1", "marketing_start_date": "19990615"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (51672-4026-2)", "package_ndc": "51672-4026-2", "marketing_start_date": "19990615"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (51672-4026-6)", "package_ndc": "51672-4026-6", "marketing_end_date": "20260831", "marketing_start_date": "19990615"}, {"sample": false, "description": "3 BLISTER PACK in 1 BOX (51672-4026-8)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "51672-4026-8", "marketing_start_date": "19990615"}, {"sample": false, "description": "5 BLISTER PACK in 1 BOX (51672-4026-9)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "51672-4026-9", "marketing_start_date": "19990615"}], "brand_name": "Ketoconazole", "product_id": "51672-4026_3dd44662-95fb-0d34-e063-6294a90a5fbc", "dosage_form": "TABLET", "pharm_class": ["Azole Antifungal [EPC]", "Azoles [CS]", "Cytochrome P450 3A4 Inhibitors [MoA]", "Cytochrome P450 3A5 Inhibitors [MoA]", "P-Glycoprotein Inhibitors [MoA]"], "product_ndc": "51672-4026", "generic_name": "Ketoconazole", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ketoconazole", "active_ingredients": [{"name": "KETOCONAZOLE", "strength": "200 mg/1"}], "application_number": "ANDA075319", "marketing_category": "ANDA", "marketing_start_date": "19990615", "listing_expiration_date": "20261231"}