Sertraline Hydrochloride

Product NDC
84386-099
11-digit product format
843860099
Labeler code
84386
Product ID
84386-099_b497dfeb-a48c-4f2a-b309-b56f3a26a19b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sertraline Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Aurobindo Pharma Limited
Application
ANDA077206
Marketing category
ANDA
Marketing start
2025-11-20
Substance
SERTRALINE HYDROCHLORIDE
Active strength
100 mg/1
Pharmacologic classes
Cytochrome P450 2D6 Inhibitors [MoA], Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
UTI8907Y6XSERTRALINE HYDROCHLORIDE79559-97-0SERTRALINE HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
84386-099-0184386009901100 TABLET, FILM COATED in 1 BOTTLE (84386-099-01) 2025-11-20NoNoHistorical
84386-099-0584386009905500 TABLET, FILM COATED in 1 BOTTLE (84386-099-05) 2025-11-20NoNoHistorical
84386-099-25843860099252500 TABLET, FILM COATED in 1 BOTTLE (84386-099-25) 2025-11-20NoNoHistorical
84386-099-308438600993030 TABLET, FILM COATED in 1 BOTTLE (84386-099-30) 2025-11-20NoNoHistorical
84386-099-508438600995050 TABLET, FILM COATED in 1 BOTTLE (84386-099-50) 2025-11-20NoNoHistorical
84386-099-608438600996060 TABLET, FILM COATED in 1 BOTTLE (84386-099-60) 2025-11-20NoNoHistorical
84386-099-908438600999090 TABLET, FILM COATED in 1 BOTTLE (84386-099-90) 2025-11-20NoNoHistorical
84386-099-99843860099991000 TABLET, FILM COATED in 1 BOTTLE (84386-099-99) 2025-11-20NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Sertraline HydrochlorideAurobindo Pharma Limited | APL HEALTHCARE LIMITED2025-11-24Human Prescription Drug Label1