NDC 70518-3923 – Escitalopram

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

Human Prescription Drug

Product NDC70518-3923

Product details

Brand name
Escitalopram
Generic name
Escitalopram
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078777
Marketed since
November 22, 2023
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Escitalopram →

Package NDC codes (5)

Package NDCDescriptionSince
70518-3923-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-3923-0)Nov 22, 2023
70518-3923-190 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3923-1)Jul 29, 2024
70518-3923-260 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3923-2)Dec 4, 2024
70518-3923-330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3923-3)Jan 16, 2025
70518-3923-430 TABLET, FILM COATED in 1 BLISTER PACK (70518-3923-4)Aug 14, 2025

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