NDC 82009-035 – Escitalopram oxalate

Escitalopram Oxalate 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82009-035

Product details

Brand name
Escitalopram oxalate
Generic name
Escitalopram oxalate
Labeler
Quallent Pharmaceuticals Health LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090939
Marketed since
March 1, 2023
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
82009-035-101000 TABLET in 1 BOTTLE (82009-035-10)Mar 1, 2023

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