cefuroxime axetil
Generic: cefuroxime axetil
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
cefuroxime axetil
Generic Name
cefuroxime axetil
Labeler
american health packaging
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
cefuroxime axetil 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-272
Product ID
60687-272_3bb8ed50-e786-f167-e063-6294a90a6031
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065496
Listing Expiration
2026-12-31
Marketing Start
2018-05-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687272
Hyphenated Format
60687-272
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
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 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-272-94) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-272-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3bb8ed50-e786-f167-e063-6294a90a6031", "openfda": {"unii": ["Z49QDT0J8Z"], "rxcui": ["309097", "309098"], "spl_set_id": ["f38418a7-dd90-4f20-b747-7ac086c53015"], "manufacturer_name": ["American Health Packaging"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-272-94) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-272-11)", "package_ndc": "60687-272-94", "marketing_start_date": "20180523"}], "brand_name": "Cefuroxime axetil", "product_id": "60687-272_3bb8ed50-e786-f167-e063-6294a90a6031", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "60687-272", "generic_name": "Cefuroxime axetil", "labeler_name": "American Health Packaging", "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": "20180523", "listing_expiration_date": "20261231"}