cefadroxil

Generic: cefadroxil

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefadroxil
Generic Name cefadroxil
Labeler remedyrepack inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

cefadroxil 500 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3580
Product ID 70518-3580_3ac1c1de-a1d9-da21-e063-6294a90aed29
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065392
Listing Expiration 2026-12-31
Marketing Start 2022-11-22

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183580
Hyphenated Format 70518-3580

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 ANDA065392 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 20 CAPSULE in 1 BLISTER PACK (70518-3580-0)
  • 30 CAPSULE in 1 BLISTER PACK (70518-3580-1)
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": "3ac1c1de-a1d9-da21-e063-6294a90aed29", "openfda": {"unii": ["280111G160"], "rxcui": ["309049"], "spl_set_id": ["eb365f05-1c8f-4495-b443-abb0580b39fb"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "20 CAPSULE in 1 BLISTER PACK (70518-3580-0)", "package_ndc": "70518-3580-0", "marketing_start_date": "20221122"}, {"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-3580-1)", "package_ndc": "70518-3580-1", "marketing_start_date": "20221221"}], "brand_name": "Cefadroxil", "product_id": "70518-3580_3ac1c1de-a1d9-da21-e063-6294a90aed29", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "70518-3580", "generic_name": "Cefadroxil", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefadroxil", "active_ingredients": [{"name": "CEFADROXIL", "strength": "500 mg/1"}], "application_number": "ANDA065392", "marketing_category": "ANDA", "marketing_start_date": "20221122", "listing_expiration_date": "20261231"}