escitalopram

NDC 16571-757 · Rising Pharma Holdings, 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

16571-757-01 — 100 TABLET, FILM COATED in 1 BOTTLE (16571-757-01)

16571-757-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (16571-757-10)

FDA lists these products with the same active ingredient.

0615-8475 — Escitalopram Oxalate, 0615-8476 — Escitalopram Oxalate, 0615-8477 — Escitalopram Oxalate, 0904-6426 — escitalopram, 0904-6427 — escitalopram, 13668-135 — escitalopram, 13668-136 — escitalopram, 13668-137 — escitalopram, 16571-755 — escitalopram, 16571-756 — escitalopram, 16571-769 — Escitalopram Oxalate, 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, +133 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.