NDC 51672-1348 – Escitalopram

Escitalopram Oxalate 5 mg/5mL · Solution · Oral

Human Prescription Drug

Product NDC51672-1348

Product details

Brand name
Escitalopram
Generic name
Escitalopram Oxalate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA079121
Marketed since
May 3, 2012
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for escitalopram →

Package NDC codes (3)

Package NDCDescriptionSince
51672-1348-11 BOTTLE in 1 CARTON (51672-1348-1) / 240 mL in 1 BOTTLEMay 3, 2012
51672-1348-81 BOTTLE in 1 CARTON (51672-1348-8) / 120 mL in 1 BOTTLEMay 3, 2012
51672-1348-91 BOTTLE in 1 CARTON (51672-1348-9) / 480 mL in 1 BOTTLEMay 3, 2012

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