NDC 76420-762 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 30 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC76420-762

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone Hydrochloride
Labeler
Asclemed USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091490
Marketed since
September 8, 2014
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
76420-762-01100 TABLET in 1 BOTTLE, PLASTIC (76420-762-01)Jan 8, 2025
76420-762-1010 TABLET in 1 BOTTLE, PLASTIC (76420-762-10)Jan 8, 2025
76420-762-2020 TABLET in 1 BOTTLE, PLASTIC (76420-762-20)Jan 8, 2025
76420-762-3030 TABLET in 1 BOTTLE, PLASTIC (76420-762-30)Jan 8, 2025
76420-762-6060 TABLET in 1 BOTTLE, PLASTIC (76420-762-60)Jan 8, 2025
76420-762-9090 TABLET in 1 BOTTLE, PLASTIC (76420-762-90)Jan 8, 2025

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