Package 68788-8655-1

Brand: cefdinir

Generic: cefdinir
NDC Package

Package Facts

Identity

Package NDC 68788-8655-1
Digits Only 6878886551
Product NDC 68788-8655
Product ID 68788-8655_2e81498d-8e5a-47b9-8b47-8063cf8300a1
Description

100 mL in 1 BOTTLE (68788-8655-1)

Marketing

Marketing Status
Marketed Since 2024-05-09
Brand cefdinir
Generic cefdinir
Sample Package No

Linked Drug Pages (1)

Cefdinir ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2e81498d-8e5a-47b9-8b47-8063cf8300a1", "openfda": {"unii": ["6E7SN358SE"], "rxcui": ["476576"], "spl_set_id": ["0d1212c9-604f-4999-8f7d-e7cf300705ef"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68788-8655-1)", "package_ndc": "68788-8655-1", "marketing_start_date": "20240509"}], "brand_name": "Cefdinir", "product_id": "68788-8655_2e81498d-8e5a-47b9-8b47-8063cf8300a1", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68788-8655", "generic_name": "Cefdinir", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefdinir", "active_ingredients": [{"name": "CEFDINIR MONOHYDRATE", "strength": "250 mg/5mL"}], "application_number": "ANDA065332", "marketing_category": "ANDA", "marketing_start_date": "20240509", "listing_expiration_date": "20261231"}