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Buprenorphine and Naloxone

NDC 3215-6523 · Aveva Drug Delivery Systems Inc.

Generic namebuprenorphine and naloxone

Dosage formFILM

RouteBUCCAL, SUBLINGUAL

Active ingredient(s)BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE

Strength8; 2 mg/1; mg/1

Pharmacologic classOpioid Antagonist [EPC], Opioid Antagonists [MoA], Partial Opioid Agonist [EPC], Partial Opioid Agonists [MoA]

DEA scheduleCIII

Marketing categoryANDA

Packages

3215-6523-30 — 30 POUCH in 1 CARTON (3215-6523-30) / 1 FILM in 1 POUCH (3215-6523-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

31722-479 — buprenorphine and naloxone, 31722-480 — buprenorphine and naloxone, 31722-481 — buprenorphine and naloxone, 31722-482 — buprenorphine and naloxone, 31722-850 — Buprenorphine and Naloxone, 31722-851 — Buprenorphine and Naloxone, 31722-870 — Buprenorphine HCl, 31722-871 — Buprenorphine HCl, 3215-6521 — buprenorphine and naloxone, 3215-6522 — buprenorphine and naloxone, 3215-6524 — buprenorphine and naloxone, 36000-308 — naloxone hydrochloride, 36000-310 — NALOXONE HYDROCHLORIDE, 42023-179 — Buprenorphine Hydrochloride, 42023-224 — Naloxone Hydrochloride, 42291-493 — Naloxone Hydrochloride, 42858-501 — BUPRENORPHINE, 42858-502 — BUPRENORPHINE, 42858-601 — Buprenorphine and Naloxone, 42858-602 — Buprenorphine and Naloxone, +235 more

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