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Buprenorphine

NDC 60687-481 · American Health Packaging

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

60687-481-21 — 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-481-21) / 1 TABLET in 1 BLISTER PACK (60687-481-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 59385-024 — buprenorphine hydrochloride, 59385-025 — buprenorphine hydrochloride, 59385-026 — buprenorphine hydrochloride, 59385-027 — buprenorphine hydrochloride, 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, 63629-9475 — 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.