NDC 76420-366 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 30 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC76420-366

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone Hydrochloride
Labeler
Asclemed USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077712
Marketed since
September 10, 2024
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
76420-366-01100 TABLET in 1 BOTTLE, PLASTIC (76420-366-01)May 27, 2025
76420-366-05500 TABLET in 1 BOTTLE, PLASTIC (76420-366-05)Sep 10, 2024
76420-366-1010 TABLET in 1 BOTTLE, PLASTIC (76420-366-10)Dec 27, 2025
76420-366-3030 TABLET in 1 BOTTLE, PLASTIC (76420-366-30)May 27, 2025
76420-366-6060 TABLET in 1 BOTTLE, PLASTIC (76420-366-60)May 27, 2025
76420-366-9090 TABLET in 1 BOTTLE, PLASTIC (76420-366-90)May 27, 2025

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