NDC 68071-3600 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC68071-3600

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone Hydrochloride
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091393
Marketed since
October 18, 2013
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
68071-3600-44 TABLET in 1 BOTTLE (68071-3600-4)May 8, 2024

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