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Buprenorphine and Naloxone

NDC 50742-397 · INGENUS PHARMACEUTICALS, LLC

Generic namebuprenorphine and naloxone
Dosage formFILM
RouteBUCCAL, SUBLINGUAL
Active ingredient(s)BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE
Strength2; .5 mg/1; mg/1
Pharmacologic classOpioid Antagonist [EPC], Opioid Antagonists [MoA], Partial Opioid Agonist [EPC], Partial Opioid Agonists [MoA]
DEA scheduleCIII
Marketing categoryANDA

Packages

50742-397-30 — 30 POUCH in 1 CARTON (50742-397-30) / 1 FILM in 1 POUCH (50742-397-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-6491 — naloxone hydrochloride, 50090-6710 — naloxone hydrochloride, 50090-6963 — naloxone hydrochloride, 50090-7559 — buprenorphine hydrochloride, 50268-128 — Buprenorphine, 50268-129 — Buprenorphine, 50268-144 — Buprenorphine and Naloxone, 50268-145 — Buprenorphine and Naloxone, 50742-364 — buprenorphine and naloxone, 50742-365 — buprenorphine and naloxone, 50742-398 — buprenorphine and naloxone, 51316-210 — Naloxone Hydrochloride, 51407-948 — buprenorphine hydrochloride and naloxone hydrochloride dihydrate, 51407-949 — buprenorphine hydrochloride and naloxone hydrochloride dihydrate, 51662-1238 — NALOXONE HYDROCHLORIDE, 51662-1239 — NALOXONE HYDROCHLORIDE, 51662-1240 — NARCAN NALOXONE HCI, 51662-1242 — NALOXONE HCI, 51662-1385 — NALOXONE HYDROCHLORIDE, 51662-1426 — NALOXONE HYDROCHLORIDE, +235 more

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