FDA.reportPublic FDA data

Cefuroxime axetil

Product NDC
67296-2168
11-digit product format
672962168
Labeler code
67296
Product ID
67296-2168_45abddff-8c57-a374-e063-6294a90a83ea
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cefuroxime axetil
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Redpharm Drug
Application
ANDA065496
Marketing category
ANDA
Marketing start
2010-12-01
Substance
CEFUROXIME AXETIL
Active strength
500 mg/1
Pharmacologic classes
Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Cefuroxime axetil
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CEFUROXIME AXETIL500 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiZ49QDT0J8Z
Rxcui309098

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ba66f2a7-7ba5-e81a-8863-a38bd5c2e969Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67296-2168-7Cefuroxime axetil14 in 1 BOTTLETABLET, FILM COATED144

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
309098cefuroxime axetil 500 MG Oral TabletPSN3744f28c-c7e1-259c-e063-6294a90a10ed4
309098cefuroxime 500 MG Oral TabletSCD3744f28c-c7e1-259c-e063-6294a90a10ed4
309098cefuroxime (as cefuroxime axetil) 500 MG Oral TabletSY3744f28c-c7e1-259c-e063-6294a90a10ed4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
67296-2168-76729621680714 TABLET, FILM COATED in 1 BOTTLE (67296-2168-7) 2010-12-01NoNoCurrent