cefadroxil

Generic: cefadroxil

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefadroxil
Generic Name cefadroxil
Labeler direct rx
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

cefadroxil 500 mg/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-103
Product ID 72189-103_2be86c94-8c9d-1da3-e063-6294a90a1319
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065352
Listing Expiration 2026-12-31
Marketing Start 2020-06-12

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189103
Hyphenated Format 72189-103

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 ANDA065352 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 6 CAPSULE in 1 BOTTLE (72189-103-06)
  • 20 CAPSULE in 1 BOTTLE (72189-103-20)
source: ndc

Packages (2)

72189-103-06 6 CAPSULE in 1 BOTTLE (72189-103-06) 72189-103-20 20 CAPSULE in 1 BOTTLE (72189-103-20)

Ingredients (1)

cefadroxil (500 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": "2be86c94-8c9d-1da3-e063-6294a90a1319", "openfda": {"unii": ["280111G160"], "rxcui": ["309049"], "spl_set_id": ["a7e74b63-9d5c-7baa-e053-2a95a90a98b2"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "6 CAPSULE in 1 BOTTLE (72189-103-06)", "package_ndc": "72189-103-06", "marketing_start_date": "20200612"}, {"sample": false, "description": "20 CAPSULE in 1 BOTTLE (72189-103-20)", "package_ndc": "72189-103-20", "marketing_start_date": "20200612"}], "brand_name": "CEFADROXIL", "product_id": "72189-103_2be86c94-8c9d-1da3-e063-6294a90a1319", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "72189-103", "generic_name": "CEFADROXIL", "labeler_name": "DIRECT RX", "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": "20200612", "listing_expiration_date": "20261231"}