NDC 42858-003 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 15 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII 1 recall

Product NDC42858-003

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone Hydrochloride
Labeler
Rhodes Pharmaceuticals LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091490
Marketed since
September 8, 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
42858-003-01100 TABLET in 1 BOTTLE, PLASTIC (42858-003-01)Sep 8, 2014

Recalls mentioning this NDC

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