Citalopram Hydrobromide

Product NDC
50090-2888
11-digit product format
500902888
Labeler code
50090
Product ID
50090-2888_e64d836f-e882-4ccb-a0f0-c6c3964e004e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Citalopram Hydrobromide
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA078216
Marketing category
ANDA
Marketing start
2007-10-18
Marketing end
0000-00-00
Substance
CITALOPRAM HYDROBROMIDE
Active strength
10 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50090-2888-02020-01-31C16284748780-19d75b9d0-55d5-f424-e053-dadaa90a57ce47a080c4-a685-4634-9acf-37a4aa60c178

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2888-0EA - Each50090-288887f43af4-6fac-426c-95fc-fac6320af26012019-04-11