Citalopram Hydrobromide

Product NDC
50090-2774
11-digit product format
500902774
Labeler code
50090
Product ID
50090-2774_ec2b07ca-10f7-4a9e-9e93-36e7b3e3cc93
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
50090-2774-02020-01-31C16284748780-19d75b9cf-d2b9-f424-e053-dadaa90a57ce6fe6422e-e497-4194-8433-c746d05bbce5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2774-0EA - Each50090-27742bbe8569-f1f2-46de-8096-4edfbd36e03e12019-04-11