cefadroxil
Generic: cefadroxil
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
cefadroxil
Generic Name
cefadroxil
Labeler
remedyrepack inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
cefadroxil 500 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183580
Hyphenated Format
70518-3580
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 20 CAPSULE in 1 BLISTER PACK (70518-3580-0)
- 30 CAPSULE in 1 BLISTER PACK (70518-3580-1)
Packages (2)
Ingredients (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"}