Buprenorphine and Naloxone
NDC 62175-458 · Lannett Company, Inc.
Generic nameBuprenorphine and Naloxone
Dosage formTABLET
RouteSUBLINGUAL
Active ingredient(s)BUPRENORPHINE, NALOXONE
Strength8; 2 mg/1; mg/1
Pharmacologic classOpioid Antagonist [EPC], Opioid Antagonists [MoA], Partial Opioid Agonist [EPC], Partial Opioid Agonists [MoA]
DEA scheduleCIII
Marketing categoryANDA
Packages
62175-458-32 — 30 TABLET in 1 BOTTLE (62175-458-32)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
58284-208 — BUPRENORPHINE, 58284-216 — BUPRENORPHINE, 58284-224 — BUPRENORPHINE, 58284-228 — BUPRENORPHINE, 58284-232 — BUPRENORPHINE, 58284-264 — BUPRENORPHINE, 58284-296 — BUPRENORPHINE, 59011-750 — buprenorphine, 59011-751 — buprenorphine, 59011-752 — buprenorphine, 59011-757 — buprenorphine, 59011-758 — buprenorphine, 62175-452 — Buprenorphine and Naloxone, 69238-1202 — Buprenorphine, 69238-1203 — Buprenorphine, 69238-1204 — Buprenorphine, 69238-1205 — Buprenorphine, 69238-1505 — Buprenorphine, 71335-1296 — Buprenorphine and Naloxone, 71335-1378 — Buprenorphine and Naloxone, +31 more