cefuroxime axetil

Generic: cefuroxime axetil

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefuroxime axetil
Generic Name cefuroxime axetil
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cefuroxime axetil 250 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-623
Product ID 43063-623_4139bcab-48f4-70b8-e063-6394a90a0267
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065308
Listing Expiration 2026-12-31
Marketing Start 2006-03-29

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43063623
Hyphenated Format 43063-623

Supplemental Identifiers

RxCUI
309097
UPC
0343063623145
UNII
Z49QDT0J8Z

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 cefuroxime axetil (source: ndc)
Generic Name cefuroxime axetil (source: ndc)
Application Number ANDA065308 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 14 TABLET in 1 BOTTLE, PLASTIC (43063-623-14)
  • 20 TABLET in 1 BOTTLE, PLASTIC (43063-623-20)
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-623-30)
source: ndc

Packages (3)

Ingredients (1)

cefuroxime axetil (250 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4139bcab-48f4-70b8-e063-6394a90a0267", "openfda": {"upc": ["0343063623145"], "unii": ["Z49QDT0J8Z"], "rxcui": ["309097"], "spl_set_id": ["a84ac4ed-c268-4e9f-9df8-256e0a64cd16"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (43063-623-14)", "package_ndc": "43063-623-14", "marketing_start_date": "20241010"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (43063-623-20)", "package_ndc": "43063-623-20", "marketing_start_date": "20151027"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-623-30)", "package_ndc": "43063-623-30", "marketing_start_date": "20151027"}], "brand_name": "Cefuroxime Axetil", "product_id": "43063-623_4139bcab-48f4-70b8-e063-6394a90a0267", "dosage_form": "TABLET", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "43063-623", "generic_name": "Cefuroxime Axetil", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefuroxime Axetil", "active_ingredients": [{"name": "CEFUROXIME AXETIL", "strength": "250 mg/1"}], "application_number": "ANDA065308", "marketing_category": "ANDA", "marketing_start_date": "20060329", "listing_expiration_date": "20261231"}