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Butrans

NDC 59011-751 · Knoa Pharma LLC

Generic namebuprenorphine
Dosage formPATCH, EXTENDED RELEASE
RouteTRANSDERMAL
Active ingredient(s)BUPRENORPHINE
Strength10 ug/h
Pharmacologic classPartial Opioid Agonist [EPC], Partial Opioid Agonists [MoA]
DEA scheduleCIII
Marketing categoryNDA

Packages

59011-751-04 — 4 POUCH in 1 CARTON (59011-751-04) / 1 PATCH in 1 POUCH / 168 h in 1 PATCH

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50742-376 — Buprenorphine, 58064-408 — buprenorphine, 58284-208 — BUPRENORPHINE, 58284-216 — BUPRENORPHINE, 58284-224 — BUPRENORPHINE, 58284-228 — BUPRENORPHINE, 58284-232 — BUPRENORPHINE, 58284-264 — BUPRENORPHINE, 58284-296 — BUPRENORPHINE, 59011-750 — buprenorphine, 59011-752 — buprenorphine, 59011-757 — buprenorphine, 59011-758 — buprenorphine, 62175-452 — Buprenorphine and Naloxone, 62175-458 — Buprenorphine and Naloxone, 69238-1202 — Buprenorphine, 69238-1203 — Buprenorphine, 69238-1204 — Buprenorphine, 69238-1205 — Buprenorphine, 69238-1505 — Buprenorphine, +27 more

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