NDC 0115-1560 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 40 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC0115-1560

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone Hydrochloride
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA022272
Marketed since
February 22, 2016
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0115-1560-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0115-1560-01)Feb 22, 2016

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