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NDC 64896-0696-08 Oxymorphone hydrochloride 7.5 mg/1 Details

Oxymorphone hydrochloride 7.5 mg/1

Oxymorphone hydrochloride is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals LLC. The primary component is OXYMORPHONE HYDROCHLORIDE.

MedlinePlus Drug Summary

Oxymorphone is used to relieve moderate to severe pain in people whose pain is not controlled with other medications. Oxymorphone is in a class of medications called opiate (narcotic) analgesics. It works by changing the way the body responds to pain.

Related Packages: 64896-0696-08
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Oxymorphone

Product Information

NDC	64896-0696
Product ID	64896-696_61a770cc-7bae-4c2f-8db8-b8219c64e681
Associated GPIs	65100080107407
GCN Sequence Number	063782
GCN Sequence Number Description	oxymorphone HCl TAB ER 12H 7.5 MG ORAL
HIC3	H3A
HIC3 Description	OPIOID ANALGESICS
GCN	99492
HICL Sequence Number	001696
HICL Sequence Number Description	OXYMORPHONE HCL
Brand/Generic	Generic
Proprietary Name	Oxymorphone hydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	Oxymorphone hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	7.5
Active Ingredient Units	mg/1
Substance Name	OXYMORPHONE HYDROCHLORIDE
Labeler Name	Amneal Pharmaceuticals LLC
Pharmaceutical Class	Full Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA Schedule	CII
Marketing Category	ANDA
Application Number	ANDA079087
Listing Certified Through	2024-12-31

Package

NDC 64896-0696-08 (64896069608)

Pricing Information	N/A
NDC Package Code	64896-696-08
Billing NDC	64896069608
Package	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-08)
Marketing Start Date	2013-01-02
NDC Exclude Flag	N