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Buprenorphine HCl

NDC 31722-870 · Camber Pharmaceuticals, Inc.

Generic nameBuprenorphine HCl
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

31722-870-30 — 30 TABLET in 1 BOTTLE (31722-870-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

12496-1208 — buprenorphine hydrochloride, naloxone hydrochloride, 12496-1212 — buprenorphine hydrochloride, naloxone hydrochloride, 16729-549 — BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE, 16729-550 — BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE, 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, 31722-871 — Buprenorphine HCl, 3215-6521 — buprenorphine and naloxone, 3215-6522 — buprenorphine and naloxone, 3215-6523 — buprenorphine and naloxone, 3215-6524 — buprenorphine and naloxone, 42023-179 — Buprenorphine Hydrochloride, 42858-501 — BUPRENORPHINE, 42858-502 — BUPRENORPHINE, 42858-601 — Buprenorphine and Naloxone, 42858-602 — Buprenorphine and Naloxone, +139 more

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