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BELBUCA

NDC 59385-022 · BioDelivery Sciences International Inc

Generic namebuprenorphine hydrochloride
Dosage formFILM, SOLUBLE
RouteBUCCAL
Active ingredient(s)BUPRENORPHINE HYDROCHLORIDE
Strength150 ug/1
Pharmacologic classPartial Opioid Agonist [EPC], Partial Opioid Agonists [MoA]
DEA scheduleCIII
Marketing categoryNDA

Packages

59385-022-60 — 60 POUCH in 1 CARTON (59385-022-60) / 1 FILM, SOLUBLE in 1 POUCH (59385-022-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

58118-0460 — Buprenorphine, 58118-0501 — BUPRENORPHINE, 58118-0502 — BUPRENORPHINE, 58118-0549 — BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE, 58118-1188 — buprenorphine hydrochloride and naloxone hydrochloride dihydrate, 58118-1189 — buprenorphine hydrochloride and naloxone hydrochloride dihydrate, 58118-4459 — Buprenorphine, 58118-8005 — Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate, 58118-8020 — Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate, 59385-021 — buprenorphine hydrochloride, 59385-023 — buprenorphine hydrochloride, 59385-024 — buprenorphine hydrochloride, 59385-025 — buprenorphine hydrochloride, 59385-026 — buprenorphine hydrochloride, 59385-027 — buprenorphine hydrochloride, 60687-481 — Buprenorphine, 60687-492 — Buprenorphine, 60687-626 — Buprenorphine and Naloxone, 60687-637 — Buprenorphine and Naloxone, 62756-459 — Buprenorphine, +139 more

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