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Nortriptyline Hydrochloride

NDC 70710-1156 · Zydus Pharmaceuticals (USA) Inc.

Generic nameNortriptyline Hydrochloride
Dosage formCAPSULE
RouteORAL
Active ingredient(s)NORTRIPTYLINE HYDROCHLORIDE
Strength75 mg/1
Pharmacologic classTricyclic Antidepressant [EPC]
Marketing categoryANDA

Packages

70710-1156-1 — 100 CAPSULE in 1 BOTTLE (70710-1156-1)

70710-1156-3 — 30 CAPSULE in 1 BOTTLE (70710-1156-3)

70710-1156-5 — 500 CAPSULE in 1 BOTTLE (70710-1156-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-8721 — Nortriptyline Hydrochloride, 68788-8900 — Nortriptyline Hydrochloride, 70518-3920 — Nortriptyline Hydrochloride, 70518-4017 — Nortriptyline Hydrochloride, 70518-4086 — Nortriptyline Hydrochloride, 70518-4122 — Nortriptyline Hydrochloride, 70518-4281 — Nortriptyline Hydrochloride, 70710-1153 — Nortriptyline Hydrochloride, 70710-1154 — Nortriptyline Hydrochloride, 70710-1155 — Nortriptyline Hydrochloride, 70771-1612 — Nortriptyline Hydrochloride, 70771-1613 — Nortriptyline Hydrochloride, 70771-1614 — Nortriptyline Hydrochloride, 70771-1615 — Nortriptyline Hydrochloride, 71205-254 — Nortriptyline Hydrochloride, 71205-770 — Nortriptyline Hydrochloride, 71335-0065 — Nortriptyline Hydrochloride, 71335-0083 — Nortriptyline Hydrochloride, 71335-0155 — Nortriptyline Hydrochloride, 71335-0426 — Nortriptyline Hydrochloride, +63 more

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