NDC 65862-374 – Escitalopram

Escitalopram Oxalate 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC65862-374

Product details

Brand name
Escitalopram
Generic name
Escitalopram Oxalate
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090432
Marketed since
September 11, 2012
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Escitalopram →

Package NDC codes (6)

Package NDCDescriptionSince
65862-374-01100 TABLET, FILM COATED in 1 BOTTLE (65862-374-01)Sep 11, 2012
65862-374-05500 TABLET, FILM COATED in 1 BOTTLE (65862-374-05)Sep 11, 2012
65862-374-1010 BLISTER PACK in 1 CARTON (65862-374-10) / 10 TABLET, FILM COATED in 1 BLISTER PACKSep 11, 2012
65862-374-3030 TABLET, FILM COATED in 1 BOTTLE (65862-374-30)Sep 11, 2012
65862-374-595000 TABLET, FILM COATED in 1 BOTTLE (65862-374-59)Sep 11, 2012
65862-374-9090 TABLET, FILM COATED in 1 BOTTLE (65862-374-90)Sep 11, 2012

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