NDC 70518-2226 – Buprenorphine HCl

Buprenorphine Hydrochloride 2 mg/1 · Tablet · Sublingual

Human Prescription Drug DEA schedule CIII

Product NDC70518-2226

Product details

Brand name
Buprenorphine HCl
Generic name
Buprenorphine HCl
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Sublingual
Marketing category
ANDA · ANDA078633
Marketed since
July 19, 2019
Listing expires
December 31, 2027
Pharmacologic class
Partial Opioid Agonist

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
70518-2226-030 TABLET in 1 BLISTER PACK (70518-2226-0)Jul 19, 2019
70518-2226-5100 POUCH in 1 BOX (70518-2226-5) / 1 TABLET in 1 POUCH (70518-2226-6)Jul 13, 2026

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