NDC 72189-580 – Buprenorphine Sublingual C-III

Buprenorphine Hydrochloride 2 mg/1 · Tablet · Sublingual

Human Prescription Drug DEA schedule CIII

Product NDC72189-580

Product details

Brand name
Buprenorphine Sublingual C-III
Generic name
Buprenorphine Sublingual C-III
Labeler
Direct_Rx
Dosage form
Tablet
Route
Sublingual
Marketing category
ANDA · ANDA078633
Marketed since
September 16, 2024
Listing expires
December 31, 2026
Pharmacologic class
Partial Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Buprenorphine Sublingual C-III →

Package NDC codes (2)

Package NDCDescriptionSince
72189-580-6060 TABLET in 1 BOTTLE (72189-580-60)Sep 16, 2024
72189-580-9090 TABLET in 1 BOTTLE (72189-580-90)Sep 16, 2024

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