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MORPHINE SULFATE - 42549-659-60 - (MORPHINE SULFATE)

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Drug Information of MORPHINE SULFATE

Product NDC: 42549-659
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
Coding System: National Drug Codes(NDC)

Labeler Information of MORPHINE SULFATE

Product NDC: 42549-659
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022207
Marketing Category: NDA
Start Marketing Date: 20080317

Package Information of MORPHINE SULFATE

Package NDC: 42549-659-60
Package Description: 60 TABLET in 1 BOTTLE (42549-659-60)

NDC Information of MORPHINE SULFATE

NDC Code 42549-659-60
Proprietary Name MORPHINE SULFATE
Package Description 60 TABLET in 1 BOTTLE (42549-659-60)
Product NDC 42549-659
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MORPHINE SULFATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080317
Marketing Category Name NDA
Labeler Name STAT Rx USA LLC
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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