NDC 67296-2123 – Buprenorphine HCl

Buprenorphine Hydrochloride 2 mg/1 · Tablet · Sublingual

Human Prescription Drug DEA schedule CIII

Product NDC67296-2123

Product details

Brand name
Buprenorphine HCl
Generic name
Buprenorphine HCl
Labeler
Redpharm Drug
Dosage form
Tablet
Route
Sublingual
Marketing category
ANDA · ANDA078633
Marketed since
October 8, 2009
Listing expires
December 31, 2026
Pharmacologic class
Partial Opioid Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
67296-2123-330 TABLET in 1 BOTTLE (67296-2123-3)Oct 8, 2009

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