Package 68180-181-02

Brand: cefadroxil

Generic: cefadroxil
NDC Package

Package Facts

Identity

Package NDC 68180-181-02
Digits Only 6818018102
Product NDC 68180-181
Product ID 68180-181_3818bd15-cf3a-4b07-bef5-57169a33a170
Description

100 mL in 1 BOTTLE (68180-181-02)

Marketing

Marketing Status
Marketed Since 2008-04-23
Brand cefadroxil
Generic cefadroxil
Sample Package No

Linked Drug Pages (1)

Cefadroxil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3818bd15-cf3a-4b07-bef5-57169a33a170", "openfda": {"unii": ["280111G160"], "rxcui": ["105171", "309048"], "spl_set_id": ["27009a05-4d2b-4618-be76-39f348240eda"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68180-181-02)", "package_ndc": "68180-181-02", "marketing_start_date": "20080423"}], "brand_name": "Cefadroxil", "product_id": "68180-181_3818bd15-cf3a-4b07-bef5-57169a33a170", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68180-181", "generic_name": "Cefadroxil", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefadroxil", "active_ingredients": [{"name": "CEFADROXIL", "strength": "250 mg/5mL"}], "application_number": "ANDA065396", "marketing_category": "ANDA", "marketing_start_date": "20080423", "listing_expiration_date": "20261231"}