cefadroxil

Generic: cefadroxil

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefadroxil
Generic Name cefadroxil
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cefadroxil 1000 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-4059
Product ID 0093-4059_980978a7-5c16-4350-add2-dd7c88ecb91b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062774
Listing Expiration 2026-12-31
Marketing Start 2007-01-31

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00934059
Hyphenated Format 0093-4059

Supplemental Identifiers

RxCUI
309047
UNII
280111G160

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name cefadroxil (source: ndc)
Generic Name cefadroxil (source: ndc)
Application Number ANDA062774 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 50 TABLET in 1 BOTTLE (0093-4059-53)
source: ndc

Packages (1)

0093-4059-53 50 TABLET in 1 BOTTLE (0093-4059-53)

Ingredients (1)

cefadroxil (1000 mg/1)

Linked Drug Pages (1)

Cefadroxil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "980978a7-5c16-4350-add2-dd7c88ecb91b", "openfda": {"unii": ["280111G160"], "rxcui": ["309047"], "spl_set_id": ["4674a05c-fdef-4737-a4b8-e3229bdada9d"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (0093-4059-53)", "package_ndc": "0093-4059-53", "marketing_start_date": "20070131"}], "brand_name": "Cefadroxil", "product_id": "0093-4059_980978a7-5c16-4350-add2-dd7c88ecb91b", "dosage_form": "TABLET", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0093-4059", "generic_name": "Cefadroxil", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefadroxil", "active_ingredients": [{"name": "CEFADROXIL", "strength": "1000 mg/1"}], "application_number": "ANDA062774", "marketing_category": "ANDA", "marketing_start_date": "20070131", "listing_expiration_date": "20261231"}