cefadroxil
Generic: cefadroxil
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
cefadroxil
Generic Name
cefadroxil
Labeler
preferred pharmaceuticals inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
cefadroxil 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8479
Product ID
68788-8479_11ebff6b-9531-4032-a078-0fbf7fa0f997
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065352
Listing Expiration
2026-12-31
Marketing Start
2023-07-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888479
Hyphenated Format
68788-8479
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
ANDA065352 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 20 CAPSULE in 1 BOTTLE (68788-8479-2)
- 30 CAPSULE in 1 BOTTLE (68788-8479-3)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "11ebff6b-9531-4032-a078-0fbf7fa0f997", "openfda": {"unii": ["280111G160"], "rxcui": ["309049"], "spl_set_id": ["41bc5f5a-5e1d-4cb6-a795-9f1756a8f074"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 CAPSULE in 1 BOTTLE (68788-8479-2)", "package_ndc": "68788-8479-2", "marketing_start_date": "20230713"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68788-8479-3)", "package_ndc": "68788-8479-3", "marketing_start_date": "20230713"}], "brand_name": "Cefadroxil", "product_id": "68788-8479_11ebff6b-9531-4032-a078-0fbf7fa0f997", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68788-8479", "generic_name": "Cefadroxil", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20230713", "listing_expiration_date": "20261231"}