Package 68071-3156-6

Brand: cefdinir

Generic: cefdinir
NDC Package

Package Facts

Identity

Package NDC 68071-3156-6
Digits Only 6807131566
Product NDC 68071-3156
Description

60 mL in 1 BOTTLE (68071-3156-6)

Marketing

Marketing Status
Marketed Since 2017-03-16
Brand cefdinir
Generic cefdinir
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d53fd8c-5f3f-8b3f-e063-6394a90a3ea0", "openfda": {"upc": ["0368071315660"], "unii": ["6E7SN358SE"], "rxcui": ["309054"], "spl_set_id": ["4ade94bb-6c39-13cd-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 BOTTLE (68071-3156-6)", "package_ndc": "68071-3156-6", "marketing_start_date": "20170316"}], "brand_name": "Cefdinir", "product_id": "68071-3156_2d53fd8c-5f3f-8b3f-e063-6394a90a3ea0", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68071-3156", "generic_name": "Cefdinir", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefdinir", "active_ingredients": [{"name": "CEFDINIR MONOHYDRATE", "strength": "125 mg/5mL"}], "application_number": "ANDA065332", "marketing_category": "ANDA", "marketing_start_date": "20070508", "listing_expiration_date": "20261231"}