cefadroxil
Generic: cefadroxil
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
cefadroxil
Generic Name
cefadroxil
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
cefadroxil 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43063-595
Product ID
43063-595_41399346-37b8-2396-e063-6394a90ae471
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065352
Listing Expiration
2026-12-31
Marketing Start
2007-01-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43063595
Hyphenated Format
43063-595
Supplemental Identifiers
RxCUI
UPC
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, PLASTIC (43063-595-20)
- 28 CAPSULE in 1 BOTTLE, PLASTIC (43063-595-28)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41399346-37b8-2396-e063-6394a90ae471", "openfda": {"upc": ["0343063595206"], "unii": ["280111G160"], "rxcui": ["309049"], "spl_set_id": ["ab9cf28c-7c16-4bfa-879d-c360b4d1d5a6"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 CAPSULE in 1 BOTTLE, PLASTIC (43063-595-20)", "package_ndc": "43063-595-20", "marketing_start_date": "20150817"}, {"sample": false, "description": "28 CAPSULE in 1 BOTTLE, PLASTIC (43063-595-28)", "package_ndc": "43063-595-28", "marketing_start_date": "20160721"}], "brand_name": "Cefadroxil", "product_id": "43063-595_41399346-37b8-2396-e063-6394a90ae471", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "43063-595", "generic_name": "Cefadroxil", "labeler_name": "PD-Rx 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": "20070125", "listing_expiration_date": "20261231"}