Citalopram

Product NDC
59746-544
11-digit product format
597460544
Labeler code
59746
Product ID
59746-544_4aa4fe4e-9862-49ef-8370-c0d91a955601
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
citalopram hydrobromide
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Jubilant Cadista Pharmaceuticals Inc.
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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59746-544-01EA - Each59746-544e2134994-0acc-4c29-8a98-2afce4a0a55f12016-09-02
59746-544-05EA - Each59746-5445f6d79dd-6ee1-49ba-a3d4-4de4c7f4093512016-09-02