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Morphine Sulfate - 0832-0230-00 - (Morphine Sulfate)

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Drug Information of Morphine Sulfate

Product NDC: 0832-0230
Proprietary Name: Morphine Sulfate
Non Proprietary Name: Morphine Sulfate
Active Ingredient(s): 80    mg/1 & nbsp;   Morphine Sulfate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Morphine Sulfate

Product NDC: 0832-0230
Labeler Name: Upsher-Smith Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202104
Marketing Category: ANDA
Start Marketing Date: 20130630

Package Information of Morphine Sulfate

Package NDC: 0832-0230-00
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0832-0230-00)

NDC Information of Morphine Sulfate

NDC Code 0832-0230-00
Proprietary Name Morphine Sulfate
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0832-0230-00)
Product NDC 0832-0230
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Morphine Sulfate
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130630
Marketing Category Name ANDA
Labeler Name Upsher-Smith Laboratories, Inc.
Substance Name MORPHINE SULFATE
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Morphine Sulfate


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