NDC 82111-203 – Zubsolv

Buprenorphine Hydrochloride 2.9 mg/1; Naloxone Hydrochloride .71 mg/1 · Tablet, Orally Disintegrating · Sublingual

Human Prescription Drug DEA schedule CIII

Product NDC82111-203

Product details

Brand name
Zubsolv
Generic name
Buprenorphine hydrochloride and naloxone hydrochloride
Labeler
Edenbridge Pharmaceuticals LLC.
Dosage form
Tablet, Orally Disintegrating
Route
Sublingual
Marketing category
NDA · NDA204242
Marketed since
June 12, 2026
Listing expires
December 31, 2027
Pharmacologic class
Opioid Antagonist; Partial Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Zubsolv →

Package NDC codes (1)

Package NDCDescriptionSince
82111-203-303 BLISTER PACK in 1 CARTON (82111-203-30) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKJun 12, 2026

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