Diazepam

NDC 76420-783 · Asclemed USA, Inc.

Generic nameDiazepam

Dosage formTABLET

RouteORAL

Active ingredient(s)DIAZEPAM

Strength2 mg/1

Pharmacologic classBenzodiazepine [EPC], Benzodiazepines [CS]

DEA scheduleCIV

Marketing categoryANDA

Packages

76420-783-01 100 TABLET in 1 BOTTLE (76420-783-01)

76420-783-02 2 TABLET in 1 BOTTLE (76420-783-02)

76420-783-03 3 TABLET in 1 BOTTLE (76420-783-03)

76420-783-05 5 TABLET in 1 BOTTLE (76420-783-05)

76420-783-10 10 TABLET in 1 BOTTLE (76420-783-10)

76420-783-20 20 TABLET in 1 BOTTLE (76420-783-20)

76420-783-30 30 TABLET in 1 BOTTLE (76420-783-30)

76420-783-55 500 TABLET in 1 BOTTLE (76420-783-55)

76420-783-60 60 TABLET in 1 BOTTLE (76420-783-60)

76420-783-90 90 TABLET in 1 BOTTLE (76420-783-90)

FDA lists these products with the same active ingredient.

72252-505 — diazepam, 72252-510 — diazepam, 72252-515 — diazepam, 72252-520 — diazepam, 72572-140 — DIAZEPAM, 76045-204 — DIAZEPAM, 76420-314 — DIAZEPAM, 76420-315 — DIAZEPAM, 76420-316 — DIAZEPAM, 76420-533 — Diazepam, 76420-784 — Diazepam, 80425-0120 — Diazepam, 80425-0496 — diazepam, 80425-0511 — DIAZEPAM, 80425-0512 — diazepam, 80725-004 — Diazepam, 80725-005 — Diazepam, 80725-006 — Diazepam, 82804-186 — DIAZEPAM, 87441-025 — diazepam, +106 more

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