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Morphine Sulfate - 0409-3815-12 - (Morphine Sulfate)

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Drug Information of Morphine Sulfate

Product NDC: 0409-3815
Proprietary Name: Morphine Sulfate
Non Proprietary Name: Morphine Sulfate
Active Ingredient(s): 1    mg/mL & nbsp;   Morphine Sulfate
Administration Route(s): EPIDURAL; INTRATHECAL; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Morphine Sulfate

Product NDC: 0409-3815
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073510
Marketing Category: ANDA
Start Marketing Date: 20120305

Package Information of Morphine Sulfate

Package NDC: 0409-3815-12
Package Description: 5 VIAL, GLASS in 1 CARTON (0409-3815-12) > 10 mL in 1 VIAL, GLASS

NDC Information of Morphine Sulfate

NDC Code 0409-3815-12
Proprietary Name Morphine Sulfate
Package Description 5 VIAL, GLASS in 1 CARTON (0409-3815-12) > 10 mL in 1 VIAL, GLASS
Product NDC 0409-3815
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Morphine Sulfate
Dosage Form Name INJECTION, SOLUTION
Route Name EPIDURAL; INTRATHECAL; INTRAVENOUS
Start Marketing Date 20120305
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name MORPHINE SULFATE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Morphine Sulfate


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