DIAZEPAM

NDC 76420-315 · ASCLEMED USA INC.

Generic nameDIAZEPAM

Dosage formTABLET

RouteORAL

Active ingredient(s)DIAZEPAM

Strength5 mg/1

Pharmacologic classBenzodiazepine [EPC], Benzodiazepines [CS]

DEA scheduleCIV

Marketing categoryANDA

Packages

76420-315-00 1000 TABLET in 1 BOTTLE (76420-315-00)

76420-315-01 100 TABLET in 1 BOTTLE (76420-315-01)

76420-315-05 500 TABLET in 1 BOTTLE (76420-315-05)

76420-315-10 10 TABLET in 1 BOTTLE (76420-315-10)

76420-315-20 20 TABLET in 1 BOTTLE (76420-315-20)

76420-315-30 30 TABLET in 1 BOTTLE (76420-315-30)

76420-315-60 60 TABLET in 1 BOTTLE (76420-315-60)

76420-315-90 90 TABLET in 1 BOTTLE (76420-315-90)

FDA lists these products with the same active ingredient.

71872-7260 — DIAZEPAM, 72189-552 — Diazepam, 72189-570 — Diazepam, 72252-505 — diazepam, 72252-510 — diazepam, 72252-515 — diazepam, 72252-520 — diazepam, 72572-140 — DIAZEPAM, 76045-204 — DIAZEPAM, 76420-314 — DIAZEPAM, 76420-316 — DIAZEPAM, 76420-533 — Diazepam, 76420-783 — Diazepam, 76420-784 — Diazepam, 80425-0120 — Diazepam, 80425-0496 — diazepam, 80425-0511 — DIAZEPAM, 80425-0512 — diazepam, 80725-004 — Diazepam, 80725-005 — 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.