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BUPRENORPHINE

NDC 63629-9475 · Bryant Ranch Prepack

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

63629-9475-1 — 30 TABLET in 1 BOTTLE (63629-9475-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60687-481 — Buprenorphine, 60687-492 — Buprenorphine, 60687-626 — Buprenorphine and Naloxone, 60687-637 — Buprenorphine and Naloxone, 62756-459 — Buprenorphine, 62756-460 — Buprenorphine, 62756-969 — Buprenorphine and Naloxone, 62756-970 — Buprenorphine and Naloxone, 63629-5074 — Buprenorphine and Naloxone, 63629-7269 — Buprenorphine and Naloxone, 63629-9482 — Buprenorphine and Naloxone, 63629-9483 — Buprenorphine and Naloxone, 65162-415 — Buprenorphine and Naloxone, 65162-416 — Buprenorphine and Naloxone, 67296-1933 — Buprenorphine and Naloxone, 67296-2063 — Buprenorphine and Naloxone, 67296-2123 — Buprenorphine HCl, 67296-2164 — Buprenorphine and Naloxone, 67296-2173 — Buprenorphine, 67296-2191 — BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE, +139 more

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