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DIAZEPAM

NDC 61919-906 · Direct_Rx

Generic nameDIAZEPAM
Dosage formTABLET
RouteORAL
Active ingredient(s)DIAZEPAM
Strength10 mg/1
Pharmacologic classBenzodiazepine [EPC], Benzodiazepines [CS]
DEA scheduleCIV
Marketing categoryANDA

Packages

61919-906-02 — 2 TABLET in 1 BOTTLE (61919-906-02)

61919-906-05 — 5 TABLET in 1 BOTTLE (61919-906-05)

61919-906-10 — 10 TABLET in 1 BOTTLE (61919-906-10)

61919-906-30 — 30 TABLET in 1 BOTTLE (61919-906-30)

61919-906-60 — 60 TABLET in 1 BOTTLE (61919-906-60)

61919-906-90 — 90 TABLET in 1 BOTTLE (61919-906-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55154-5554 — diazepam, 55289-092 — diazepam, 58118-3925 — Diazepam, 58118-3926 — Diazepam, 58118-4047 — diazepam, 59651-652 — DIAZEPAM, 59651-653 — DIAZEPAM, 59651-654 — DIAZEPAM, 60687-755 — Diazepam, 61919-409 — DIAZEPAM, 62135-767 — Diazepam Oral, 62135-768 — Diazepam Oral Solution (Concentrate), 62135-786 — Diazepam, 62135-787 — Diazepam, 62135-788 — Diazepam, 62332-811 — Diazepam, 63187-173 — Diazepam, 63187-544 — Diazepam, 63629-1523 — Diazepam, 63629-2948 — 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.