Escitalopram

NDC 42708-163 · QPharma, Inc.

Generic nameEscitalopram

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)ESCITALOPRAM OXALATE

Strength20 mg/1

Pharmacologic classSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]

Marketing categoryANDA

Packages

42708-163-30 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-163-30)

FDA lists these products with the same active ingredient.

16729-168 — Escitalopram, 16729-169 — Escitalopram, 16729-170 — Escitalopram, 31722-569 — Escitalopram Oxalate, 33342-036 — Escitalopram Oxalate, 33342-037 — Escitalopram Oxalate, 33342-038 — Escitalopram Oxalate, 33342-053 — escitalopram, 42708-077 — Escitalopram Oxalate, 42708-155 — Escitalopram, 43063-661 — Escitalopram, 43063-761 — escitalopram oxalate, 43547-280 — Escitalopram, 43547-281 — Escitalopram, 43547-282 — Escitalopram, 43602-473 — escitalopram, 43602-474 — escitalopram, 43602-475 — escitalopram, 50090-4915 — Escitalopram, 50090-5312 — Escitalopram, +133 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.