NDC 42023-179 – Buprenorphine Hydrochloride

Buprenorphine Hydrochloride .324 mg/mL · Injection · Intramuscular, Intravenous

Human Prescription Drug DEA schedule CIII 4 recalls

Product NDC42023-179

Product details

Brand name
Buprenorphine Hydrochloride
Generic name
Buprenorphine Hydrochloride
Labeler
Par Health USA, LLC
Dosage form
Injection
Route
Intramuscular, Intravenous
Marketing category
ANDA · ANDA206586
Marketed since
July 30, 2015
Listing expires
December 31, 2027
Pharmacologic class
Partial Opioid Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
42023-179-055 VIAL in 1 CARTON (42023-179-05) / 1 mL in 1 VIALJul 30, 2015

Recalls mentioning this NDC

Other Buprenorphine Hydrochloride products