NDC 13107-103 – Oxymorphone Hydrochloride

Oxymorphone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC13107-103

Product details

Brand name
Oxymorphone Hydrochloride
Generic name
Oxymorphone Hydrochloride
Labeler
Aurolife Pharma, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204459
Marketed since
April 26, 2016
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
13107-103-01100 TABLET in 1 BOTTLE (13107-103-01)Apr 26, 2016
13107-103-3030 TABLET in 1 BOTTLE (13107-103-30)Apr 26, 2016
13107-103-991000 TABLET in 1 BOTTLE (13107-103-99)Apr 26, 2016

Other Oxymorphone Hydrochloride products