Sertraline Hydrochloride

Product NDC
76420-786
11-digit product format
764200786
Labeler code
76420
Product ID
76420-786_2dffc9e0-9a6b-2d51-e063-6294a90ac7be
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sertraline Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Asclemed USA, Inc.
Application
ANDA077206
Marketing category
ANDA
Marketing start
2007-02-06
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
76420-786-0176420078601100 TABLET, FILM COATED in 1 BOTTLE (76420-786-01) 2024-03-14NoNoHistorical
76420-786-307642007863030 TABLET, FILM COATED in 1 BOTTLE (76420-786-30) 2024-03-14NoNoHistorical
76420-786-607642007866060 TABLET, FILM COATED in 1 BOTTLE (76420-786-60) 2024-03-14NoNoHistorical
76420-786-907642007869090 TABLET, FILM COATED in 1 BOTTLE (76420-786-90) 2024-03-14NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Sertraline HydrochlorideAsclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2025-02-12HUMAN PRESCRIPTION DRUG LABEL2