cefadroxil
Generic: cefadroxil
Labeler: northstar rx llcDrug Facts
Product Profile
Brand Name
cefadroxil
Generic Name
cefadroxil
Labeler
northstar rx llc
Dosage Form
CAPSULE
Routes
Active Ingredients
cefadroxil 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
16714-388
Product ID
16714-388_f043b17c-7588-4594-904b-056efaea3446
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
16714388
Hyphenated Format
16714-388
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
ANDA065352 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 50 CAPSULE in 1 BOTTLE (16714-388-01)
- 100 CAPSULE in 1 BOTTLE (16714-388-02)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f043b17c-7588-4594-904b-056efaea3446", "openfda": {"unii": ["280111G160"], "rxcui": ["309049"], "spl_set_id": ["17123057-58c7-401a-b87d-8c4c0764bbf6"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 CAPSULE in 1 BOTTLE (16714-388-01)", "package_ndc": "16714-388-01", "marketing_start_date": "20070125"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (16714-388-02)", "package_ndc": "16714-388-02", "marketing_start_date": "20070125"}], "brand_name": "Cefadroxil", "product_id": "16714-388_f043b17c-7588-4594-904b-056efaea3446", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "16714-388", "generic_name": "Cefadroxil", "labeler_name": "NorthStar Rx LLC", "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"}