cefadroxil
Generic: cefadroxil
Labeler: direct_rxDrug Facts
Product Profile
Brand Name
cefadroxil
Generic Name
cefadroxil
Labeler
direct_rx
Dosage Form
CAPSULE
Routes
Active Ingredients
cefadroxil 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72189-445
Product ID
72189-445_2c4d982f-27ee-a7c8-e063-6394a90a9af0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065392
Listing Expiration
2026-12-31
Marketing Start
2023-03-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189445
Hyphenated Format
72189-445
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
- 6 CAPSULE in 1 BOTTLE (72189-445-06)
- 20 CAPSULE in 1 BOTTLE (72189-445-20)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4d982f-27ee-a7c8-e063-6394a90a9af0", "openfda": {"unii": ["280111G160"], "rxcui": ["309049"], "spl_set_id": ["f6ddd84a-4a44-7035-e053-6294a90a6606"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "6 CAPSULE in 1 BOTTLE (72189-445-06)", "package_ndc": "72189-445-06", "marketing_start_date": "20230314"}, {"sample": false, "description": "20 CAPSULE in 1 BOTTLE (72189-445-20)", "package_ndc": "72189-445-20", "marketing_start_date": "20230314"}], "brand_name": "Cefadroxil", "product_id": "72189-445_2c4d982f-27ee-a7c8-e063-6394a90a9af0", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "72189-445", "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": "ANDA065392", "marketing_category": "ANDA", "marketing_start_date": "20230314", "listing_expiration_date": "20261231"}