cefadroxil
Generic: cefadroxil
Labeler: teva pharmaceuticals usa, inc.Drug Facts
Product Profile
Brand Name
cefadroxil
Generic Name
cefadroxil
Labeler
teva pharmaceuticals usa, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
cefadroxil 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0093-3196
Product ID
0093-3196_86b8951f-3699-4888-9eeb-7bbda995ec35
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065282
Listing Expiration
2026-12-31
Marketing Start
2007-01-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00933196
Hyphenated Format
0093-3196
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA065282 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (0093-3196-01)
- 50 CAPSULE in 1 BOTTLE (0093-3196-53)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "86b8951f-3699-4888-9eeb-7bbda995ec35", "openfda": {"unii": ["280111G160"], "rxcui": ["309049"], "spl_set_id": ["bda86975-8c2f-4c4e-9a4c-a1a959f9336a"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0093-3196-01)", "package_ndc": "0093-3196-01", "marketing_start_date": "20070131"}, {"sample": false, "description": "50 CAPSULE in 1 BOTTLE (0093-3196-53)", "package_ndc": "0093-3196-53", "marketing_start_date": "20070131"}], "brand_name": "Cefadroxil", "product_id": "0093-3196_86b8951f-3699-4888-9eeb-7bbda995ec35", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0093-3196", "generic_name": "Cefadroxil", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefadroxil", "active_ingredients": [{"name": "CEFADROXIL", "strength": "500 mg/1"}], "application_number": "ANDA065282", "marketing_category": "ANDA", "marketing_start_date": "20070131", "listing_expiration_date": "20261231"}