NDC 70752-136 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 5 mg/5mL · Solution · Oral

Human Prescription Drug DEA schedule CII

Product NDC70752-136

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone Hydrochloride
Labeler
QUAGEN PHARMACEUTICALS LLC
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA213761
Marketed since
June 2, 2021
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
70752-136-101 BOTTLE, PLASTIC in 1 CARTON (70752-136-10) / 100 mL in 1 BOTTLE, PLASTICJun 2, 2021
70752-136-141 BOTTLE, PLASTIC in 1 CARTON (70752-136-14) / 500 mL in 1 BOTTLE, PLASTICJun 2, 2021

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