Home > National Drug Code (NDC) > Morphine Sulfate

Morphine Sulfate - 49999-849-30 - (Morphine Sulfate)

Alphabetical Index


Drug Information of Morphine Sulfate

Product NDC: 49999-849
Proprietary Name: Morphine Sulfate
Non Proprietary Name: Morphine Sulfate
Active Ingredient(s): 30    mg/1 & nbsp;   Morphine Sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Morphine Sulfate

Product NDC: 49999-849
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022195
Marketing Category: NDA
Start Marketing Date: 20111213

Package Information of Morphine Sulfate

Package NDC: 49999-849-30
Package Description: 30 TABLET in 1 BOTTLE (49999-849-30)

NDC Information of Morphine Sulfate

NDC Code 49999-849-30
Proprietary Name Morphine Sulfate
Package Description 30 TABLET in 1 BOTTLE (49999-849-30)
Product NDC 49999-849
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Morphine Sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111213
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name MORPHINE SULFATE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Morphine Sulfate


General Information