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Escitalopram Oxalate

NDC 69097-848 · Cipla USA Inc.

Generic nameEscitalopram
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ESCITALOPRAM OXALATE
Strength10 mg/1
Pharmacologic classSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
Marketing categoryANDA

Packages

69097-848-02 — 30 TABLET, FILM COATED in 1 BOTTLE (69097-848-02)

69097-848-05 — 90 TABLET, FILM COATED in 1 BOTTLE (69097-848-05)

69097-848-07 — 100 TABLET, FILM COATED in 1 BOTTLE (69097-848-07)

69097-848-12 — 500 TABLET, FILM COATED in 1 BOTTLE (69097-848-12)

69097-848-15 — 1000 TABLET, FILM COATED in 1 BOTTLE (69097-848-15)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68180-137 — Escitslopram, 68645-519 — Escitalopram, 68645-520 — Escitalopram, 68788-4171 — escitalopram, 68788-7461 — Escitalopram, 68788-8371 — escitalopram oxalate, 68788-8569 — escitalopram, 68788-8723 — escitalopram, 68999-729 — Escitalopram Oral, 69097-847 — Escitalopram, 69097-849 — Escitalopram, 70518-2317 — Escitalopram, 70518-2472 — Escitalopram, 70518-2597 — Escitalopram, 70518-3923 — escitalopram, 70518-4239 — escitalopram, 70518-4300 — escitalopram, 70518-4567 — Escitalopram, 70518-4703 — Escitalopram, 71205-168 — 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.