NDC 12496-1212 – Suboxone

Buprenorphine Hydrochloride 12 mg/1; Naloxone Hydrochloride 3 mg/1 · Film, Soluble · Buccal, Sublingual

Human Prescription Drug DEA schedule CIII

Product NDC12496-1212

Product details

Brand name
Suboxone
Generic name
Buprenorphine hydrochloride, naloxone hydrochloride
Labeler
INDIVIOR INC.
Dosage form
Film, Soluble
Route
Buccal, Sublingual
Marketing category
NDA · NDA022410
Marketed since
August 24, 2012
Listing expires
December 31, 2027
Pharmacologic class
Opioid Antagonist; Partial Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Suboxone →

Package NDC codes (1)

Package NDCDescriptionSince
12496-1212-330 POUCH in 1 CARTON (12496-1212-3) / 1 FILM, SOLUBLE in 1 POUCH (12496-1212-1)Aug 24, 2012

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