NDC 76420-768 – Oxycodone hydrochloride

Oxycodone Hydrochloride 30 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC76420-768

Product details

Brand name
Oxycodone hydrochloride
Generic name
Oxycodone hydrochloride
Labeler
Asclemed USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202116
Marketed since
December 30, 2011
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
76420-768-01100 TABLET in 1 BOTTLE (76420-768-01)Jun 25, 2024
76420-768-05500 TABLET in 1 BOTTLE (76420-768-05)Jun 25, 2024
76420-768-1010 TABLET in 1 BOTTLE (76420-768-10)Jun 25, 2024
76420-768-2020 TABLET in 1 BOTTLE (76420-768-20)Jun 25, 2024
76420-768-3030 TABLET in 1 BOTTLE (76420-768-30)Jun 25, 2024
76420-768-6060 TABLET in 1 BOTTLE (76420-768-60)Jun 25, 2024
76420-768-9090 TABLET in 1 BOTTLE (76420-768-90)Jun 25, 2024

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