NDC 43386-433 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII 1 recall

Product NDC43386-433

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone Hydrochloride
Labeler
Lupin Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204021
Marketed since
June 12, 2017
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
43386-433-01100 TABLET in 1 BOTTLE (43386-433-01)Jun 12, 2017

Recalls mentioning this NDC

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