Package 81948-6250-1

Brand: cefaclor

Generic: cefaclor
NDC Package

Package Facts

Identity

Package NDC 81948-6250-1
Digits Only 8194862501
Product NDC 81948-6250
Description

150 mL in 1 BOTTLE (81948-6250-1)

Marketing

Marketing Status
Marketed Since 2022-11-01
Brand cefaclor
Generic cefaclor
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a6a7fcf7-b9dc-4dac-b127-418588586a8a", "openfda": {"unii": ["69K7K19H4L"], "rxcui": ["313888"], "spl_set_id": ["224af904-38f3-4210-a750-e21006db4c66"], "manufacturer_name": ["Azorian Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 mL in 1 BOTTLE (81948-6250-1)", "package_ndc": "81948-6250-1", "marketing_start_date": "20221101"}], "brand_name": "Cefaclor", "product_id": "81948-6250_a6a7fcf7-b9dc-4dac-b127-418588586a8a", "dosage_form": "SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "81948-6250", "generic_name": "cefaclor", "labeler_name": "Azorian Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefaclor", "active_ingredients": [{"name": "CEFACLOR", "strength": "250 mg/5mL"}], "application_number": "ANDA065412", "marketing_category": "ANDA", "marketing_start_date": "20221101", "listing_expiration_date": "20261231"}