Home > National Drug Code (NDC) > Morphine Sulfate

Morphine Sulfate - 42858-803-01 - (Morphine Sulfate)

Alphabetical Index


Drug Information of Morphine Sulfate

Product NDC: 42858-803
Proprietary Name: Morphine Sulfate
Non Proprietary Name: Morphine Sulfate
Active Ingredient(s): 60    mg/1 & nbsp;   Morphine Sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Morphine Sulfate

Product NDC: 42858-803
Labeler Name: Rhodes Pharmaceuticals L. P.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074862
Marketing Category: ANDA
Start Marketing Date: 20110114

Package Information of Morphine Sulfate

Package NDC: 42858-803-01
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42858-803-01)

NDC Information of Morphine Sulfate

NDC Code 42858-803-01
Proprietary Name Morphine Sulfate
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42858-803-01)
Product NDC 42858-803
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Morphine Sulfate
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110114
Marketing Category Name ANDA
Labeler Name Rhodes Pharmaceuticals L. P.
Substance Name MORPHINE SULFATE
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Morphine Sulfate


General Information