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DIAZEPAM

NDC 59651-652 · Aurobindo Pharma Limited

Generic nameDIAZEPAM
Dosage formTABLET
RouteORAL
Active ingredient(s)DIAZEPAM
Strength2 mg/1
Pharmacologic classBenzodiazepine [EPC], Benzodiazepines [CS]
DEA scheduleCIV
Marketing categoryANDA

Packages

59651-652-01 — 100 TABLET in 1 BOTTLE (59651-652-01)

59651-652-05 — 500 TABLET in 1 BOTTLE (59651-652-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-3390 — diazepam, 51079-284 — diazepam, 51079-285 — diazepam, 51079-286 — diazepam, 55154-5074 — diazepam, 55154-5554 — diazepam, 55289-092 — diazepam, 58118-3925 — Diazepam, 58118-3926 — Diazepam, 58118-4047 — diazepam, 59651-653 — DIAZEPAM, 59651-654 — DIAZEPAM, 60687-755 — Diazepam, 61919-409 — DIAZEPAM, 61919-906 — DIAZEPAM, 62135-767 — Diazepam Oral, 62135-768 — Diazepam Oral Solution (Concentrate), 62135-786 — Diazepam, 62135-787 — Diazepam, 62135-788 — 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.