NDC 16571-769 – Escitalopram Oxalate

Escitalopram Oxalate 5 mg/5mL · Solution · Oral

Human Prescription Drug

Product NDC16571-769

Product details

Brand name
Escitalopram Oxalate
Generic name
Escitalopram Oxalate
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA079062
Marketed since
April 3, 2012
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Escitalopram oxalate →

Package NDC codes (1)

Package NDCDescriptionSince
16571-769-24240 mL in 1 BOTTLE (16571-769-24)Apr 3, 2012

Other Escitalopram oxalate products