NDC 64950-354 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 5 mg/5mL · Solution · Oral

Human Prescription Drug DEA schedule CII 1 recall

Product NDC64950-354

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone Hydrochloride
Labeler
Genus Lifesciences Inc.
Dosage form
Solution
Route
Oral
Marketing category
NDA · NDA200535
Marketed since
September 9, 2013
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
64950-354-101 BOTTLE, PLASTIC in 1 CARTON (64950-354-10) / 100 mL in 1 BOTTLE, PLASTICSep 9, 2013
64950-354-4540 CUP, UNIT-DOSE in 1 CASE (64950-354-45) / 5 mL in 1 CUP, UNIT-DOSE (64950-354-05)Sep 9, 2013
64950-354-501 BOTTLE, PLASTIC in 1 CARTON (64950-354-50) / 500 mL in 1 BOTTLE, PLASTICSep 9, 2013
64950-354-5550 CUP, UNIT-DOSE in 1 CASE (64950-354-55) / 5 mL in 1 CUP, UNIT-DOSE (64950-354-05)Sep 9, 2013

Recalls mentioning this NDC

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