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MORPHINE SULFATE - 0406-8315-23 - (MORPHINE SULFATE)

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Drug Information of MORPHINE SULFATE

Product NDC: 0406-8315
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: 0406-8315
Labeler Name: Mallinckrodt, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076412
Marketing Category: ANDA
Start Marketing Date: 20101021

Package Information of MORPHINE SULFATE

Package NDC: 0406-8315-23
Package Description: 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0406-8315-23)

NDC Information of MORPHINE SULFATE

NDC Code 0406-8315-23
Proprietary Name MORPHINE SULFATE
Package Description 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0406-8315-23)
Product NDC 0406-8315
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MORPHINE SULFATE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20101021
Marketing Category Name ANDA
Labeler Name Mallinckrodt, 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


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