NDC 68788-8371 – Escitalopram oxalate

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

Human Prescription Drug

Product NDC68788-8371

Product details

Brand name
Escitalopram oxalate
Generic name
Escitalopram oxalate
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090939
Marketed since
February 1, 2023
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
68788-8371-1100 TABLET, FILM COATED in 1 BOTTLE (68788-8371-1)Feb 1, 2023
68788-8371-330 TABLET, FILM COATED in 1 BOTTLE (68788-8371-3)Feb 1, 2023
68788-8371-660 TABLET, FILM COATED in 1 BOTTLE (68788-8371-6)Feb 1, 2023
68788-8371-828 TABLET, FILM COATED in 1 BOTTLE (68788-8371-8)Feb 1, 2023
68788-8371-990 TABLET, FILM COATED in 1 BOTTLE (68788-8371-9)Feb 1, 2023

Other Escitalopram oxalate products