cefuroxime axetil
Generic: cefuroxime axetil
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
cefuroxime axetil
Generic Name
cefuroxime axetil
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
cefuroxime axetil 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43063-657
Product ID
43063-657_4139efd1-921a-b349-e063-6394a90a0404
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065496
Listing Expiration
2026-12-31
Marketing Start
2010-12-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43063657
Hyphenated Format
43063-657
Supplemental Identifiers
RxCUI
UPC
UNII
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
ANDA065496 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-657-20)
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-657-60)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4139efd1-921a-b349-e063-6394a90a0404", "openfda": {"upc": ["0343063657201"], "unii": ["Z49QDT0J8Z"], "rxcui": ["309097"], "spl_set_id": ["2af94304-8118-41c7-e054-00144ff8d46c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-657-20)", "package_ndc": "43063-657-20", "marketing_start_date": "20160205"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-657-60)", "package_ndc": "43063-657-60", "marketing_start_date": "20191218"}], "brand_name": "Cefuroxime axetil", "product_id": "43063-657_4139efd1-921a-b349-e063-6394a90a0404", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "43063-657", "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": "ANDA065496", "marketing_category": "ANDA", "marketing_start_date": "20101201", "listing_expiration_date": "20261231"}