NDC 0054-0390 – Oxycodone hydrochloride

Oxycodone Hydrochloride 5 mg/5mL · Solution · Oral

Human Prescription Drug DEA schedule CII 1 recall

Product NDC0054-0390

Product details

Brand name
Oxycodone hydrochloride
Generic name
Oxycodone hydrochloride
Labeler
Hikma Pharmceuticals USA Inc.
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA204037
Marketed since
September 4, 2014
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0054-0390-63500 mL in 1 BOTTLE (0054-0390-63)Sep 4, 2014

Recalls mentioning this NDC

Other Oxycodone Hydrochloride products