NDC 3215-6521 – Buprenorphine and Naloxone

Buprenorphine Hydrochloride 2 mg/1; Naloxone Hydrochloride .5 mg/1 · Film · Buccal, Sublingual

Human Prescription Drug DEA schedule CIII

Product NDC3215-6521

Product details

Brand name
Buprenorphine and Naloxone
Generic name
Buprenorphine and naloxone
Labeler
Aveva Drug Delivery Systems Inc.
Dosage form
Film
Route
Buccal, Sublingual
Marketing category
ANDA · ANDA212756
Marketed since
March 7, 2025
Listing expires
December 31, 2027
Pharmacologic class
Opioid Antagonist; Partial Opioid Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
3215-6521-3030 POUCH in 1 CARTON (3215-6521-30) / 1 FILM in 1 POUCH (3215-6521-01)Mar 7, 2025

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