BUPRENORPHINE

NDC 58118-0501 · Clinical Solutions Wholesale, LLC

Generic nameBUPRENORPHINE

Dosage formTABLET

RouteSUBLINGUAL

Active ingredient(s)BUPRENORPHINE HYDROCHLORIDE

Strength2 mg/1

Pharmacologic classPartial Opioid Agonist [EPC], Partial Opioid Agonists [MoA]

DEA scheduleCIII

Marketing categoryANDA

Packages

58118-0501-8 — 30 TABLET in 1 BLISTER PACK (58118-0501-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51407-949 — buprenorphine hydrochloride and naloxone hydrochloride dihydrate, 54123-114 — buprenorphine hydrochloride and naloxone hydrochloride, 54123-907 — buprenorphine hydrochloride and naloxone hydrochloride, 54123-914 — buprenorphine hydrochloride and naloxone hydrochloride, 54123-929 — buprenorphine hydrochloride and naloxone hydrochloride, 54123-957 — buprenorphine hydrochloride and naloxone hydrochloride, 54123-986 — buprenorphine hydrochloride and naloxone hydrochloride, 58118-0176 — Buprenorphine HCl, 58118-0177 — Buprenorphine HCl, 58118-0460 — 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, 59385-022 — buprenorphine hydrochloride, 59385-023 — buprenorphine hydrochloride, +139 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.