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Diazepam

NDC 71335-1584 · Bryant Ranch Prepack

Generic nameDiazepam
Dosage formTABLET
RouteORAL
Active ingredient(s)DIAZEPAM
Strength5 mg/1
Pharmacologic classBenzodiazepine [EPC], Benzodiazepines [CS]
DEA scheduleCIV
Marketing categoryANDA

Packages

71335-1584-0 120 TABLET in 1 BOTTLE (71335-1584-0)

71335-1584-1 12 TABLET in 1 BOTTLE (71335-1584-1)

71335-1584-2 15 TABLET in 1 BOTTLE (71335-1584-2)

71335-1584-3 20 TABLET in 1 BOTTLE (71335-1584-3)

71335-1584-4 30 TABLET in 1 BOTTLE (71335-1584-4)

71335-1584-5 60 TABLET in 1 BOTTLE (71335-1584-5)

71335-1584-6 90 TABLET in 1 BOTTLE (71335-1584-6)

71335-1584-7 10 TABLET in 1 BOTTLE (71335-1584-7)

71335-1584-8 2 TABLET in 1 BOTTLE (71335-1584-8)

71335-1584-9 1 TABLET in 1 BOTTLE (71335-1584-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69339-137 — DIAZEPAM, 70518-0014 — Diazepam, 70518-0162 — Diazepam, 70518-1713 — Diazepam, 70518-2358 — DIAZEPAM, 70518-4704 — Diazepam, 70710-2078 — Diazepam, 70710-2079 — Diazepam, 70710-2080 — Diazepam, 71335-0444 — Diazepam, 71335-2239 — diazepam, 71335-2247 — diazepam, 71335-2306 — diazepam, 71610-270 — Diazepam, 71610-424 — Diazepam, 71872-7259 — DIAZEPAM, 71872-7260 — DIAZEPAM, 72189-552 — Diazepam, 72189-570 — Diazepam, 72252-505 — diazepam, +106 more

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