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Morphine Sulfate - 0409-2029-02 - (MORPHINE SULFATE)

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Drug Information of Morphine Sulfate

Product NDC: 0409-2029
Proprietary Name: Morphine Sulfate
Non Proprietary Name: MORPHINE SULFATE
Active Ingredient(s): 1    mg/mL & nbsp;   MORPHINE SULFATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Morphine Sulfate

Product NDC: 0409-2029
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019916
Marketing Category: NDA
Start Marketing Date: 19921030

Package Information of Morphine Sulfate

Package NDC: 0409-2029-02
Package Description: 10 CARTON in 1 CONTAINER (0409-2029-02) > 1 VIAL, SINGLE-DOSE in 1 CARTON > 30 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Morphine Sulfate

NDC Code 0409-2029-02
Proprietary Name Morphine Sulfate
Package Description 10 CARTON in 1 CONTAINER (0409-2029-02) > 1 VIAL, SINGLE-DOSE in 1 CARTON > 30 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0409-2029
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MORPHINE SULFATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19921030
Marketing Category Name NDA
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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