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NDC 71335-0707-01 Morphine sulfate 60 mg/1 Details

Morphine sulfate 60 mg/1

Morphine sulfate is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is MORPHINE SULFATE.

MedlinePlus Drug Summary

Morphine is used to relieve moderate to severe pain. Morphine extended-release tablets and capsules are only used to relieve severe (around-the-clock) pain that cannot be controlled by the use of other pain medications. Morphine extended-release tablets and capsules should not be used to treat pain that can be controlled by medication that is taken as needed. Morphine is in a class of medications called opiate (narcotic) analgesics. It works by changing the way the brain and nervous system respond to pain.

Related Packages: 71335-0707-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Morphine

Product Information

NDC	71335-0707
Product ID	71335-0707_cce77429-4247-4ead-8766-8c357684d4a4
Associated GPIs	65100055100445
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Morphine sulfate
Proprietary Name Suffix	n/a
Non-Proprietary Name	morphine sulfate
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	60
Active Ingredient Units	mg/1
Substance Name	MORPHINE SULFATE
Labeler Name	Bryant Ranch Prepack
Pharmaceutical Class	Full Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA Schedule	CII
Marketing Category	ANDA
Application Number	ANDA078761
Listing Certified Through	2024-12-31

Package

NDC 71335-0707-01 (71335070701)

Pricing Information	N/A
NDC Package Code	71335-0707-1
Billing NDC	71335070701
Package	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0707-1)
Marketing Start Date	2022-02-09
NDC Exclude Flag	N