cefadroxil

Generic: cefadroxil

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefadroxil
Generic Name cefadroxil
Labeler northstar rx llc
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

cefadroxil 500 mg/5mL

Manufacturer
NorthStar Rx LLC

Identifiers & Regulatory

Product NDC 16714-390
Product ID 16714-390_323b9a4d-c8fc-4fdb-bba4-834468a0a770
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065349
Listing Expiration 2026-12-31
Marketing Start 2013-04-25

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16714390
Hyphenated Format 16714-390

Supplemental Identifiers

RxCUI
105171 309048
UPC
0316714390024 0316714389011
UNII
280111G160

Packaging Origin

Original Packager
true

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 ANDA065349 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/5mL
source: ndc
Packaging
  • 75 mL in 1 BOTTLE (16714-390-01)
  • 100 mL in 1 BOTTLE (16714-390-02)
source: ndc

Packages (2)

Ingredients (1)

cefadroxil (500 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "323b9a4d-c8fc-4fdb-bba4-834468a0a770", "openfda": {"upc": ["0316714390024", "0316714389011"], "unii": ["280111G160"], "rxcui": ["105171", "309048"], "spl_set_id": ["30bb3686-87b4-4676-9ff5-e20deb8bff9d"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "75 mL in 1 BOTTLE (16714-390-01)", "package_ndc": "16714-390-01", "marketing_start_date": "20130425"}, {"sample": false, "description": "100 mL in 1 BOTTLE (16714-390-02)", "package_ndc": "16714-390-02", "marketing_start_date": "20130425"}], "brand_name": "Cefadroxil", "product_id": "16714-390_323b9a4d-c8fc-4fdb-bba4-834468a0a770", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "16714-390", "generic_name": "Cefadroxil", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefadroxil", "active_ingredients": [{"name": "CEFADROXIL", "strength": "500 mg/5mL"}], "application_number": "ANDA065349", "marketing_category": "ANDA", "marketing_start_date": "20130425", "listing_expiration_date": "20261231"}