Buprenorphine
NDC 0093-3659 · Teva Pharmaceuticals USA, Inc.
Generic nameBuprenorphine
Dosage formPATCH, EXTENDED RELEASE
RouteTRANSDERMAL
Active ingredient(s)BUPRENORPHINE
Strength20 ug/h
Pharmacologic classPartial Opioid Agonist [EPC], Partial Opioid Agonists [MoA]
DEA scheduleCIII
Marketing categoryANDA
Packages
0093-3659-40 — 4 POUCH in 1 CARTON (0093-3659-40) / 1 PATCH in 1 POUCH / 168 h in 1 PATCH
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
0093-3239 — Buprenorphine, 0093-3656 — Buprenorphine, 0093-3657 — Buprenorphine, 0093-3658 — Buprenorphine, 12496-0100 — buprenorphine, 12496-0300 — buprenorphine, 3215-1521 — Buprenorphine, 3215-1522 — Buprenorphine, 3215-1523 — Buprenorphine, 3215-1524 — Buprenorphine, 3215-1525 — Buprenorphine, 42858-353 — 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, +27 more