cefadroxil

Generic: cefadroxil

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefadroxil
Generic Name cefadroxil
Labeler rising pharma holdings, inc.
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

cefadroxil 500 mg/5mL

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 57237-098
Product ID 57237-098_59b4c983-458c-4363-b2e6-4253a2bc7992
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 57237098
Hyphenated Format 57237-098

Supplemental Identifiers

RxCUI
105171 309048
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
  • 100 mL in 1 BOTTLE (57237-098-01)
  • 75 mL in 1 BOTTLE (57237-098-75)
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": "59b4c983-458c-4363-b2e6-4253a2bc7992", "openfda": {"unii": ["280111G160"], "rxcui": ["105171", "309048"], "spl_set_id": ["6e4111d3-f11b-403c-b340-b216022709df"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (57237-098-01)", "package_ndc": "57237-098-01", "marketing_start_date": "20130425"}, {"sample": false, "description": "75 mL in 1 BOTTLE (57237-098-75)", "package_ndc": "57237-098-75", "marketing_start_date": "20130425"}], "brand_name": "Cefadroxil", "product_id": "57237-098_59b4c983-458c-4363-b2e6-4253a2bc7992", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "57237-098", "generic_name": "Cefadroxil", "labeler_name": "Rising Pharma Holdings, Inc.", "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"}