NDC 87441-003 – Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate

Buprenorphine Hydrochloride 2 mg/1; Naloxone Hydrochloride Dihydrate .5 mg/1 · Tablet · Sublingual

Human Prescription Drug DEA schedule CIII

Product NDC87441-003

Product details

Brand name
Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate
Generic name
Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate
Labeler
Unit Dose Solutions, Inc.
Dosage form
Tablet
Route
Sublingual
Marketing category
ANDA · ANDA207000
Marketed since
April 13, 2026
Listing expires
December 31, 2027
Pharmacologic class
Opioid Antagonist; Partial Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE →

Package NDC codes (1)

Package NDCDescriptionSince
87441-003-0130 TABLET in 1 BLISTER PACK (87441-003-01)Apr 13, 2026

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