Sertraline

Product NDC
68071-4400
11-digit product format
680714400
Labeler code
68071
Product ID
68071-4400_d5d0b340-3350-b4f9-e053-2995a90a0cbd
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sertraline
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA077670
Marketing category
ANDA
Marketing start
2007-02-06
Marketing end
0000-00-00
Substance
SERTRALINE HYDROCHLORIDE
Active strength
50 mg/1
Pharmacologic classes
Cytochrome P450 2D6 Inhibitors [MoA], Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68071-4400-26807144000220 TABLET, FILM COATED in 1 BOTTLE (68071-4400-2) 2018-04-190000-00-00NoNoCurrent
68071-4400-36807144000330 TABLET, FILM COATED in 1 BOTTLE (68071-4400-3) 2018-04-190000-00-00NoNoCurrent
68071-4400-56807144000556 TABLET, FILM COATED in 1 BOTTLE (68071-4400-5) 2018-04-190000-00-00NoNoCurrent
68071-4400-66807144000660 TABLET, FILM COATED in 1 BOTTLE (68071-4400-6) 2018-04-190000-00-00NoNoCurrent
68071-4400-86807144000828 TABLET, FILM COATED in 1 BOTTLE (68071-4400-8) 2018-04-190000-00-00NoNoCurrent
68071-4400-96807144000990 TABLET, FILM COATED in 1 BOTTLE (68071-4400-9) 2018-04-190000-00-00NoNoCurrent