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Morphine Sulfate - 0409-6179-14 - (MORPHINE SULFATE)

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Drug Information of Morphine Sulfate

Product NDC: 0409-6179
Proprietary Name: Morphine Sulfate
Non Proprietary Name: MORPHINE SULFATE
Active Ingredient(s): 25    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: 0409-6179
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19910411

Package Information of Morphine Sulfate

Package NDC: 0409-6179-14
Package Description: 1 VIAL in 1 CARTON (0409-6179-14) > 10 mL in 1 VIAL

NDC Information of Morphine Sulfate

NDC Code 0409-6179-14
Proprietary Name Morphine Sulfate
Package Description 1 VIAL in 1 CARTON (0409-6179-14) > 10 mL in 1 VIAL
Product NDC 0409-6179
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MORPHINE SULFATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19910411
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Hospira, Inc.
Substance Name MORPHINE SULFATE
Strength Number 25
Strength Unit mg/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Morphine Sulfate


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