NDC 70518-1557 – Buprenorphine

Buprenorphine Hydrochloride 2 mg/1 · Tablet · Sublingual

Human Prescription Drug DEA schedule CIII

Product NDC70518-1557

Product details

Brand name
Buprenorphine
Generic name
Buprenorphine
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Sublingual
Marketing category
ANDA · ANDA090819
Marketed since
October 19, 2018
Listing expires
December 31, 2027
Pharmacologic class
Partial Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Buprenorphine →

Package NDC codes (1)

Package NDCDescriptionSince
70518-1557-150 POUCH in 1 BOX (70518-1557-1) / 1 TABLET in 1 POUCH (70518-1557-2)Jul 7, 2026

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