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Morphine Sulfate - 66689-033-16 - (Morphine Sulfate)

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Drug Information of Morphine Sulfate

Product NDC: 66689-033
Proprietary Name: Morphine Sulfate
Non Proprietary Name: Morphine Sulfate
Active Ingredient(s): 20    mg/5mL & nbsp;   Morphine Sulfate
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Morphine Sulfate

Product NDC: 66689-033
Labeler Name: VistaPharm Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201947
Marketing Category: ANDA
Start Marketing Date: 20120301

Package Information of Morphine Sulfate

Package NDC: 66689-033-16
Package Description: 500 mL in 1 BOTTLE (66689-033-16)

NDC Information of Morphine Sulfate

NDC Code 66689-033-16
Proprietary Name Morphine Sulfate
Package Description 500 mL in 1 BOTTLE (66689-033-16)
Product NDC 66689-033
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Morphine Sulfate
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20120301
Marketing Category Name ANDA
Labeler Name VistaPharm Inc.
Substance Name MORPHINE SULFATE
Strength Number 20
Strength Unit mg/5mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Morphine Sulfate


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