NDC 58284-232 – Brixadi

Buprenorphine 32 mg/.64mL · Injection · Subcutaneous

Human Prescription Drug DEA schedule CIII

Product NDC58284-232

Product details

Brand name
Brixadi
Generic name
Buprenorphine
Labeler
Braeburn Inc.
Dosage form
Injection
Route
Subcutaneous
Marketing category
NDA · NDA210136
Marketed since
June 6, 2023
Listing expires
December 31, 2027
Pharmacologic class
Partial Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Brixadi →

Package NDC codes (1)

Package NDCDescriptionSince
58284-232-011 SYRINGE, GLASS in 1 CARTON (58284-232-01) / .64 mL in 1 SYRINGE, GLASSJun 6, 2023

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