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Triazolam

NDC 59762-3718 · Mylan Pharmaceuticals Inc.

Generic nametriazolam
Dosage formTABLET
RouteORAL
Active ingredient(s)TRIAZOLAM
Strength.25 mg/1
Pharmacologic classBenzodiazepine [EPC], Benzodiazepines [CS]
DEA scheduleCIV
Marketing categoryNDA AUTHORIZED GENERIC

Packages

59762-3718-3 — 500 TABLET in 1 BOTTLE (59762-3718-3)

59762-3718-9 — 100 TABLET in 1 BOTTLE (59762-3718-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43353-451 — triazolam, 50090-6471 — Triazolam, 50090-7787 — Triazolam, 50742-645 — Triazolam, 50742-646 — Triazolam, 59762-3717 — triazolam, 70710-1289 — Triazolam, 70710-1521 — Triazolam, 70771-1162 — Triazolam, 70771-1576 — Triazolam, 71335-1876 — Triazolam, 72789-349 — Triazolam, 82804-275 — Triazolam

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels