Citalopram

Product NDC
50090-3247
11-digit product format
500903247
Labeler code
50090
Product ID
50090-3247_14d0d816-0fd7-49d7-9bec-a85753046cb9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
citalopram hydrobromide
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA205407
Marketing category
ANDA
Marketing start
2015-12-23
Marketing end
0000-00-00
Substance
CITALOPRAM HYDROBROMIDE
Active strength
20 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-3247-0EA - Each50090-324737cd8100-d07a-401e-b44b-951f2b44b99612019-05-02
50090-3247-1EA - Each50090-324770acb9e0-8774-4ca8-ac81-ea6c9d582d0812019-05-02
50090-3247-2EA - Each50090-3247820ef5eb-dba7-4855-afbb-310c412b05e312019-05-02
50090-3247-3EA - Each50090-3247605c5a95-0723-4bce-a95c-12a6b002acd112019-05-02