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Morphine Sulfate - 63629-4483-1 - (Morphine Sulfate)

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Drug Information of Morphine Sulfate

Product NDC: 63629-4483
Proprietary Name: Morphine Sulfate
Non Proprietary Name: Morphine Sulfate
Active Ingredient(s): 15    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: 63629-4483
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074862
Marketing Category: ANDA
Start Marketing Date: 20110114

Package Information of Morphine Sulfate

Package NDC: 63629-4483-1
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-4483-1)

NDC Information of Morphine Sulfate

NDC Code 63629-4483-1
Proprietary Name Morphine Sulfate
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-4483-1)
Product NDC 63629-4483
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 20110114
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name MORPHINE SULFATE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Morphine Sulfate


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