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MORPHINE SULFATE - 63629-3975-1 - (MORPHINE SULFATE)

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Drug Information of MORPHINE SULFATE

Product NDC: 63629-3975
Proprietary Name: MORPHINE SULFATE
Non Proprietary Name: MORPHINE SULFATE
Active Ingredient(s): 60    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: 63629-3975
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076412
Marketing Category: ANDA
Start Marketing Date: 20101021

Package Information of MORPHINE SULFATE

Package NDC: 63629-3975-1
Package Description: 90 TABLET in 1 BOTTLE (63629-3975-1)

NDC Information of MORPHINE SULFATE

NDC Code 63629-3975-1
Proprietary Name MORPHINE SULFATE
Package Description 90 TABLET in 1 BOTTLE (63629-3975-1)
Product NDC 63629-3975
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MORPHINE SULFATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101021
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name MORPHINE SULFATE
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of MORPHINE SULFATE


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