cefadroxil

Generic: cefadroxil

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefadroxil
Generic Name cefadroxil
Labeler redpharm drug
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

cefadroxil 500 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-2199
Product ID 67296-2199_45ac01b1-b5b8-6fc1-e063-6394a90a271a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065282
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 672962199
Hyphenated Format 67296-2199

Supplemental Identifiers

RxCUI
309049
UNII
280111G160

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 ANDA065282 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 14 CAPSULE in 1 BOTTLE (67296-2199-1)
source: ndc

Packages (1)

Ingredients (1)

cefadroxil (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45ac01b1-b5b8-6fc1-e063-6394a90a271a", "openfda": {"unii": ["280111G160"], "rxcui": ["309049"], "spl_set_id": ["45ac01b1-b5b7-6fc1-e063-6394a90a271a"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "14 CAPSULE in 1 BOTTLE (67296-2199-1)", "package_ndc": "67296-2199-1", "marketing_start_date": "20070131"}], "brand_name": "Cefadroxil", "product_id": "67296-2199_45ac01b1-b5b8-6fc1-e063-6394a90a271a", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "67296-2199", "generic_name": "Cefadroxil", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefadroxil", "active_ingredients": [{"name": "CEFADROXIL", "strength": "500 mg/1"}], "application_number": "ANDA065282", "marketing_category": "ANDA", "marketing_start_date": "20070131", "listing_expiration_date": "20261231"}