NDC 67296-0425 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC67296-0425

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone hydrochloride
Labeler
Redpharm Drug
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076758
Marketed since
June 30, 2004
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
67296-0425-120 TABLET in 1 BOTTLE (67296-0425-1)Jan 1, 2019
67296-0425-26 TABLET in 1 BOTTLE (67296-0425-2)Jun 30, 2004
67296-0425-310 TABLET in 1 BOTTLE (67296-0425-3)Jun 30, 2004
67296-0425-44 TABLET in 1 BOTTLE (67296-0425-4)Jan 1, 2019
67296-0425-512 TABLET in 1 BOTTLE (67296-0425-5)Jun 30, 2004
67296-0425-840 TABLET in 1 BOTTLE (67296-0425-8)Jun 30, 2004

Other Oxycodone Hydrochloride products