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Buprenorphine

NDC 62756-460 · Sun Pharmaceutical Industries, Inc.

Generic nameBuprenorphine
Dosage formTABLET
RouteSUBLINGUAL
Active ingredient(s)BUPRENORPHINE HYDROCHLORIDE
Strength8 mg/1
Pharmacologic classPartial Opioid Agonist [EPC], Partial Opioid Agonists [MoA]
DEA scheduleCIII
Marketing categoryANDA

Packages

62756-460-64 — 3 BLISTER PACK in 1 CARTON (62756-460-64) / 10 TABLET in 1 BLISTER PACK

62756-460-83 — 30 TABLET in 1 BOTTLE (62756-460-83)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 62756-969 — Buprenorphine and Naloxone, 62756-970 — Buprenorphine and Naloxone, 63629-5074 — Buprenorphine and Naloxone, 63629-7269 — Buprenorphine and Naloxone, 63629-9475 — BUPRENORPHINE, 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, +139 more

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