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
68788-8261
Product ID
68788-8261_68d80871-d8f9-40f9-9a59-7037e2943a5c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065392
Listing Expiration
2026-12-31
Marketing Start
2022-09-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888261
Hyphenated Format
68788-8261
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
- 50 CAPSULE in 1 BOTTLE (68788-8261-2)
- 30 CAPSULE in 1 BOTTLE (68788-8261-3)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "68d80871-d8f9-40f9-9a59-7037e2943a5c", "openfda": {"unii": ["280111G160"], "rxcui": ["309049"], "spl_set_id": ["485bc35b-637a-426b-aaa2-023c664914ae"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "50 CAPSULE in 1 BOTTLE (68788-8261-2)", "package_ndc": "68788-8261-2", "marketing_start_date": "20220919"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68788-8261-3)", "package_ndc": "68788-8261-3", "marketing_start_date": "20220919"}], "brand_name": "Cefadroxil", "product_id": "68788-8261_68d80871-d8f9-40f9-9a59-7037e2943a5c", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68788-8261", "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": "ANDA065392", "marketing_category": "ANDA", "marketing_start_date": "20220919", "listing_expiration_date": "20261231"}