Buprenorphine
NDC 42858-353 · Rhodes Pharmaceuticals LLC
Generic nameBuprenorphine
Dosage formPATCH
RouteTRANSDERMAL
Active ingredient(s)BUPRENORPHINE
Strength7.5 ug/h
Pharmacologic classPartial Opioid Agonist [EPC], Partial Opioid Agonists [MoA]
DEA scheduleCIII
Marketing categoryNDA AUTHORIZED GENERIC
Packages
42858-353-40 — 4 POUCH in 1 CARTON (42858-353-40) / 1 PATCH in 1 POUCH / 168 h in 1 PATCH
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
0093-3657 — Buprenorphine, 0093-3658 — Buprenorphine, 0093-3659 — Buprenorphine, 12496-0100 — buprenorphine, 12496-0300 — buprenorphine, 3215-1521 — Buprenorphine, 3215-1522 — Buprenorphine, 3215-1523 — Buprenorphine, 3215-1524 — Buprenorphine, 3215-1525 — Buprenorphine, 42858-493 — Buprenorphine, 42858-586 — Buprenorphine, 42858-750 — Buprenorphine, 42858-839 — Buprenorphine, 47781-406 — buprenorphine, 47781-407 — buprenorphine, 47781-408 — buprenorphine, 47781-419 — buprenorphine, 50742-372 — Buprenorphine, 50742-373 — Buprenorphine, +27 more