Package 68071-1637-2
Brand: cefuroxime axetil
Generic: cefuroxime axetilPackage Facts
Identity
Package NDC
68071-1637-2
Digits Only
6807116372
Product NDC
68071-1637
Description
20 TABLET, FILM COATED in 1 BOTTLE (68071-1637-2)
Marketing
Marketing Status
Brand
cefuroxime axetil
Generic
cefuroxime axetil
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1d4dd896-0f51-9c23-e063-6294a90a6f83", "openfda": {"upc": ["0368071163728"], "unii": ["Z49QDT0J8Z"], "rxcui": ["309098"], "spl_set_id": ["83476d51-be74-748b-e053-2a91aa0a3d36"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-1637-2)", "package_ndc": "68071-1637-2", "marketing_start_date": "20190304"}], "brand_name": "Cefuroxime axetil", "product_id": "68071-1637_1d4dd896-0f51-9c23-e063-6294a90a6f83", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68071-1637", "generic_name": "Cefuroxime axetil", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefuroxime axetil", "active_ingredients": [{"name": "CEFUROXIME AXETIL", "strength": "500 mg/1"}], "application_number": "ANDA065496", "marketing_category": "ANDA", "marketing_start_date": "20101201", "listing_expiration_date": "20261231"}