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 CAPSULE
Routes
ORAL
Active Ingredients

cefadroxil 500 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-085
Product ID 65862-085_58128541-059d-4ef1-9dbf-98fa1befdcf0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065352
Listing Expiration 2026-12-31
Marketing Start 2007-01-25

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65862085
Hyphenated Format 65862-085

Supplemental Identifiers

RxCUI
309049
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 ANDA065352 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (65862-085-01)
  • 50 CAPSULE in 1 BOTTLE (65862-085-50)
source: ndc

Packages (2)

Ingredients (1)

cefadroxil (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "58128541-059d-4ef1-9dbf-98fa1befdcf0", "openfda": {"unii": ["280111G160"], "rxcui": ["309049"], "spl_set_id": ["7bb90096-14d3-400e-94d3-048bff6b1292"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (65862-085-01)", "package_ndc": "65862-085-01", "marketing_start_date": "20070125"}, {"sample": false, "description": "50 CAPSULE in 1 BOTTLE (65862-085-50)", "package_ndc": "65862-085-50", "marketing_start_date": "20070125"}], "brand_name": "Cefadroxil", "product_id": "65862-085_58128541-059d-4ef1-9dbf-98fa1befdcf0", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "65862-085", "generic_name": "Cefadroxil", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefadroxil", "active_ingredients": [{"name": "CEFADROXIL", "strength": "500 mg/1"}], "application_number": "ANDA065352", "marketing_category": "ANDA", "marketing_start_date": "20070125", "listing_expiration_date": "20261231"}