Package 0093-1087-01

Brand: cefaclor

Generic: cefaclor
NDC Package

Package Facts

Identity

Package NDC 0093-1087-01
Digits Only 0093108701
Product NDC 0093-1087
Product ID 0093-1087_61ec00e0-d37d-4aa4-8f50-031ee7a37ecc
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-1087-01)

Marketing

Marketing Status
Marketed Since 2002-09-26
Brand cefaclor
Generic cefaclor
Sample Package No

Linked Drug Pages (1)

Cefaclor ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "61ec00e0-d37d-4aa4-8f50-031ee7a37ecc", "openfda": {"unii": ["69K7K19H4L"], "rxcui": ["309043"], "spl_set_id": ["0878bdc2-0410-4938-9890-96523aa81c2f"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-1087-01)", "package_ndc": "0093-1087-01", "marketing_start_date": "20020926"}], "brand_name": "Cefaclor", "product_id": "0093-1087_61ec00e0-d37d-4aa4-8f50-031ee7a37ecc", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0093-1087", "generic_name": "Cefaclor", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefaclor", "active_ingredients": [{"name": "CEFACLOR", "strength": "500 mg/1"}], "application_number": "ANDA065058", "marketing_category": "ANDA", "marketing_start_date": "20020926", "listing_expiration_date": "20261231"}