NDC 76420-757 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC76420-757

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
76420-757-01100 TABLET in 1 BOTTLE, PLASTIC (76420-757-01)Jan 8, 2024
76420-757-1010 TABLET in 1 BOTTLE, PLASTIC (76420-757-10)Jan 8, 2024
76420-757-2020 TABLET in 1 BOTTLE, PLASTIC (76420-757-20)Jan 8, 2024
76420-757-3030 TABLET in 1 BOTTLE, PLASTIC (76420-757-30)Jan 8, 2024
76420-757-6060 TABLET in 1 BOTTLE, PLASTIC (76420-757-60)Jan 8, 2024
76420-757-9090 TABLET in 1 BOTTLE, PLASTIC (76420-757-90)Jan 8, 2024

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