NDC 64896-696 – Oxymorphone hydrochloride

Oxymorphone Hydrochloride 7.5 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC64896-696

Product details

Brand name
Oxymorphone hydrochloride
Generic name
Oxymorphone hydrochloride
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA079087
Marketed since
January 2, 2013
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
64896-696-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-01)Jan 2, 2013
64896-696-031000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-03)Jan 2, 2013
64896-696-0830 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-08)Jan 2, 2013
64896-696-1360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-13)Jan 2, 2013

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