NDC 67296-2228 – Buprenorphine and Naloxone

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

Human Prescription Drug DEA schedule CIII

Product NDC67296-2228

Product details

Brand name
Buprenorphine and Naloxone
Generic name
Buprenorphine and naloxone
Labeler
Redpharm Drug
Dosage form
Film
Route
Buccal, Sublingual
Marketing category
ANDA · ANDA212756
Marketed since
August 29, 2023
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 (2)

Package NDCDescriptionSince
67296-2228-16 POUCH in 1 CARTON (67296-2228-1) / 1 FILM in 1 POUCHAug 8, 2024
67296-2228-330 POUCH in 1 CARTON (67296-2228-3) / 1 FILM in 1 POUCHAug 8, 2024

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