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Morphine Sulfate - 10019-179-68 - (Morphine Sulfate)

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Drug Information of Morphine Sulfate

Product NDC: 10019-179
Proprietary Name: Morphine Sulfate
Non Proprietary Name: Morphine Sulfate
Active Ingredient(s): 15    mg/mL & nbsp;   Morphine Sulfate
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Morphine Sulfate

Product NDC: 10019-179
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100526

Package Information of Morphine Sulfate

Package NDC: 10019-179-68
Package Description: 25 AMPULE in 1 BOX (10019-179-68) > 1 mL in 1 AMPULE (10019-179-37)

NDC Information of Morphine Sulfate

NDC Code 10019-179-68
Proprietary Name Morphine Sulfate
Package Description 25 AMPULE in 1 BOX (10019-179-68) > 1 mL in 1 AMPULE (10019-179-37)
Product NDC 10019-179
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Morphine Sulfate
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20100526
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Baxter Healthcare Corporation
Substance Name MORPHINE SULFATE
Strength Number 15
Strength Unit mg/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Morphine Sulfate


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