NDC 55700-174 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 15 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC55700-174

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone Hydrochloride
Labeler
Quality Care Products LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091393
Marketed since
October 18, 2013
Marketing end
July 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
55700-174-3030 TABLET in 1 BOTTLE (55700-174-30)Oct 18, 2013
55700-174-6060 TABLET in 1 BOTTLE (55700-174-60)Oct 18, 2013
55700-174-9090 TABLET in 1 BOTTLE (55700-174-90)Oct 18, 2013

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