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BUPRENORPHINE AND NALOXONE

NDC 67877-606 · Ascend Laboratories, LLC

Generic nameBUPRENORPHINE AND NALOXONE
Dosage formTABLET
RouteSUBLINGUAL
Active ingredient(s)BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE
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

67877-606-30 — 30 TABLET in 1 BOTTLE (67877-606-30)

67877-606-84 — 3 BLISTER PACK in 1 CARTON (67877-606-84) / 10 TABLET in 1 BLISTER PACK

67877-606-90 — 90 TABLET in 1 BOTTLE (67877-606-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67296-1933 — Buprenorphine and Naloxone, 67296-2063 — Buprenorphine and Naloxone, 67296-2123 — Buprenorphine HCl, 67296-2164 — Buprenorphine and Naloxone, 67296-2173 — Buprenorphine, 67296-2191 — BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE, 67296-2228 — buprenorphine and naloxone, 67457-292 — naloxone hydrochloride, 67457-299 — naloxone hydrochloride, 67457-992 — Naloxone Hydrochloride, 67877-607 — BUPRENORPHINE AND NALOXONE, 68001-645 — naloxone hydrochloride, 69238-2104 — Naloxone Hydrochloride, 69547-353 — Naloxone Hydrochloride, 69547-627 — naloxone hydrochloride nasal, 70069-027 — Buprenorphine Hydrochloride, 70069-071 — Naloxone Hydrochloride, 70069-072 — Naloxone Hydrochloride, 70385-2033 — Naloxone Hydrochloride, 70518-1557 — Buprenorphine, +235 more

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels