cefadroxil

Generic: cefadroxil

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefadroxil
Generic Name cefadroxil
Labeler aurobindo pharma limited
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

cefadroxil 500 mg/5mL

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-084
Product ID 65862-084_74923cbc-7511-447d-b6b2-b2d0e805a0f5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065349
Listing Expiration 2026-12-31
Marketing Start 2013-04-25

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65862084
Hyphenated Format 65862-084

Supplemental Identifiers

RxCUI
105171 309048
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 ANDA065349 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/5mL
source: ndc
Packaging
  • 100 mL in 1 BOTTLE (65862-084-01)
  • 50 mL in 1 BOTTLE (65862-084-50)
  • 75 mL in 1 BOTTLE (65862-084-75)
source: ndc

Packages (3)

65862-084-01 100 mL in 1 BOTTLE (65862-084-01) 65862-084-50 50 mL in 1 BOTTLE (65862-084-50) 65862-084-75 75 mL in 1 BOTTLE (65862-084-75)

Ingredients (1)

cefadroxil (500 mg/5mL)

Linked Drug Pages (1)

Cefadroxil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "74923cbc-7511-447d-b6b2-b2d0e805a0f5", "openfda": {"unii": ["280111G160"], "rxcui": ["105171", "309048"], "spl_set_id": ["776a8dbc-e68e-4732-acf4-0133dca0f54c"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (65862-084-01)", "package_ndc": "65862-084-01", "marketing_start_date": "20130425"}, {"sample": false, "description": "50 mL in 1 BOTTLE (65862-084-50)", "package_ndc": "65862-084-50", "marketing_start_date": "20130425"}, {"sample": false, "description": "75 mL in 1 BOTTLE (65862-084-75)", "package_ndc": "65862-084-75", "marketing_start_date": "20130425"}], "brand_name": "Cefadroxil", "product_id": "65862-084_74923cbc-7511-447d-b6b2-b2d0e805a0f5", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "65862-084", "generic_name": "Cefadroxil", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefadroxil", "active_ingredients": [{"name": "CEFADROXIL", "strength": "500 mg/5mL"}], "application_number": "ANDA065349", "marketing_category": "ANDA", "marketing_start_date": "20130425", "listing_expiration_date": "20261231"}