Cefdinir

Product NDC
68071-2599
11-digit product format
680712599
Labeler code
68071
Product ID
68071-2599_d336a56f-dc84-6b55-e053-2995a90ad11f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cefdinir
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA065473
Marketing category
ANDA
Marketing start
2007-12-14
Marketing end
0000-00-00
Substance
CEFDINIR
Active strength
125 mg/5mL
Pharmacologic classes
Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d3e72f63-2c41-955f-f4ce-e90c6403e67cProduct name220210729
e8e66e64-d220-99cb-44eb-0f32dc8cbda1Product name220210729

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68071-2599-6Cefdinir60 mL in 1 BOTTLEPOWDER, FOR SUSPENSION602
68071-2599-6Cefdinir1 in 1 CARTONPOWDER, FOR SUSPENSION12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68071-2599CEFDINIR POWDER, FOR SUSPENSION [NUCARE PHARMACEUTICALS,INC.]2Legacy NDC, 2 package rows20230715_d336a56f-dc85-6b55-e053-2995a90ad11f.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
309054cefdinir 125 MG in 5 mL Oral SuspensionPSNd336a56f-dc85-6b55-e053-2995a90ad11f2
309054cefdinir 25 MG/ML Oral SuspensionSCDd336a56f-dc85-6b55-e053-2995a90ad11f2
309054cefdinir 125 MG per 5 ML Oral SuspensionSYd336a56f-dc85-6b55-e053-2995a90ad11f2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68071-2599-6680712599061 BOTTLE in 1 CARTON (68071-2599-6) > 60 mL in 1 BOTTLE1 bottle2021-12-150000-00-00NoNoCurrent