SERTRALINE HYDROCHLORIDE

Product NDC
43063-411
11-digit product format
430630411
Labeler code
43063
Product ID
43063-411_8d6a6742-2c73-34da-e053-2a95a90ad94b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
sertraline hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
NDA019839
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
1992-02-11
Marketing end
0000-00-00
Substance
SERTRALINE HYDROCHLORIDE
Active strength
50 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
43063-411-30EA - Each43063-41192e77931-20eb-4570-a4a9-fe910524755712018-02-20
43063-411-60EA - Each43063-411cbd4fdae-9411-4e9d-b90d-0cb4d09ea05b12013-02-13
43063-411-90EA - Each43063-41133f8d6b4-76c7-4df8-ac17-a80cab90589e12013-08-02