NDC 0406-7018 – Buprenorphine HCl

Buprenorphine Hydrochloride 8 mg/1 · Tablet · Sublingual

Human Prescription Drug DEA schedule CIII

Product NDC0406-7018

Product details

Brand name
Buprenorphine HCl
Generic name
Buprenorphine HCl
Labeler
SpecGx LLC
Dosage form
Tablet
Route
Sublingual
Marketing category
ANDA · ANDA218473
Marketed since
January 19, 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
0406-7018-0330 TABLET in 1 BOTTLE (0406-7018-03)Jan 19, 2026

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