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Morphine Sulfate - 0378-2659-01 - (morphine sulfate)

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Drug Information of Morphine Sulfate

Product NDC: 0378-2659
Proprietary Name: Morphine Sulfate
Non Proprietary Name: morphine sulfate
Active Ingredient(s): 30    mg/1 & nbsp;   morphine sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Morphine Sulfate

Product NDC: 0378-2659
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200824
Marketing Category: ANDA
Start Marketing Date: 20130319

Package Information of Morphine Sulfate

Package NDC: 0378-2659-01
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-2659-01)

NDC Information of Morphine Sulfate

NDC Code 0378-2659-01
Proprietary Name Morphine Sulfate
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-2659-01)
Product NDC 0378-2659
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name morphine sulfate
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130319
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name MORPHINE SULFATE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Morphine Sulfate


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