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Morphine Sulfate - 54868-5132-3 - (Morphine Sulfate)

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Drug Information of Morphine Sulfate

Product NDC: 54868-5132
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Morphine Sulfate

Product NDC: 54868-5132
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075295
Marketing Category: ANDA
Start Marketing Date: 20040810

Package Information of Morphine Sulfate

Package NDC: 54868-5132-3
Package Description: 120 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5132-3)

NDC Information of Morphine Sulfate

NDC Code 54868-5132-3
Proprietary Name Morphine Sulfate
Package Description 120 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5132-3)
Product NDC 54868-5132
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Morphine Sulfate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20040810
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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


General Information