NDC 31722-482 – Buprenorphine and Naloxone

Buprenorphine Hydrochloride 12 mg/1; Naloxone Hydrochloride 3 mg/1 · Film, Soluble · Buccal, Sublingual

Human Prescription Drug DEA schedule CIII

Product NDC31722-482

Product details

Brand name
Buprenorphine and Naloxone
Generic name
Buprenorphine and naloxone
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Film, Soluble
Route
Buccal, Sublingual
Marketing category
ANDA · ANDA219850
Marketed since
May 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
Opioid Antagonist; Partial Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Buprenorphine and Naloxone →

Package NDC codes (1)

Package NDCDescriptionSince
31722-482-3030 POUCH in 1 CARTON (31722-482-30) / 1 FILM, SOLUBLE in 1 POUCH (31722-482-31)May 1, 2026

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