Cefdinir

Product NDC
50090-1028
11-digit product format
500901028
Labeler code
50090
Product ID
50090-1028_82f0fc9f-e253-4740-a45d-a1ade5d2729d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cefdinir
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA065332
Marketing category
ANDA
Marketing start
2007-05-08
Marketing end
0000-00-00
Substance
CEFDINIR MONOHYDRATE
Active strength
250 mg/5mL
Pharmacologic classes
Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50090-1028-02020-01-31C16284748780-19d75b9d0-9a63-f424-e053-dadaa90a57cec5c30769-7a7d-477d-a56c-f6505258e171

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-1028-0ML - Milliliter50090-1028489e8546-5581-4b74-a6b1-476cafa94a7412018-10-11