Sertraline

Product NDC
0143-9656
11-digit product format
001439656
Labeler code
0143
Product ID
0143-9656_e9e5e153-4b47-4297-9b92-7b175eafcac5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
sertraline hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Hikma Pharmaceuticals USA Inc.
Application
ANDA077864
Marketing category
ANDA
Marketing start
2012-11-06
Marketing end
0000-00-00
Substance
SERTRALINE HYDROCHLORIDE
Active strength
25 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
0143-9656-09EA - Each0143-9656c2f0c473-82bc-4be2-8f10-0c4b8bc7c85812013-07-02
0143-9656-30EA - Each0143-96567358a5c5-ab43-4010-893b-cbd72282de9512013-07-02