NDC 31722-871 – Buprenorphine HCl

Buprenorphine Hydrochloride 8 mg/1 · Tablet · Sublingual

Human Prescription Drug DEA schedule CIII

Product NDC31722-871

Product details

Brand name
Buprenorphine HCl
Generic name
Buprenorphine HCl
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Sublingual
Marketing category
ANDA · ANDA219401
Marketed since
January 12, 2026
Listing expires
December 31, 2027
Pharmacologic class
Partial Opioid Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
31722-871-3030 TABLET in 1 BOTTLE (31722-871-30)Jan 12, 2026

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