NDC 0121-0827 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 5 mg/5mL · Solution · Oral

Human Prescription Drug DEA schedule CII

Product NDC0121-0827

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone Hydrochloride
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA206914
Marketed since
April 8, 2019
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0121-0827-04118 mL in 1 BOTTLE (0121-0827-04)Apr 8, 2019
0121-0827-16500 mL in 1 BOTTLE (0121-0827-16)Apr 8, 2019

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