NDC 72189-579 – Buprenorphine Sublingual

Buprenorphine Hydrochloride 2 mg/1 · Tablet · Sublingual

Human Prescription Drug DEA schedule CIII

Product NDC72189-579

Product details

Brand name
Buprenorphine Sublingual
Generic name
Buprenorphine Sublingual
Labeler
Direct_rx
Dosage form
Tablet
Route
Sublingual
Marketing category
ANDA · ANDA201760
Marketed since
September 13, 2024
Listing expires
December 31, 2026
Pharmacologic class
Partial Opioid Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
72189-579-6060 TABLET in 1 BOTTLE (72189-579-60)Sep 13, 2024