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Morphine Sulfate - 49999-845-60 - (Morphine Sulfate)

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Drug Information of Morphine Sulfate

Product NDC: 49999-845
Proprietary Name: Morphine Sulfate
Non Proprietary Name: Morphine Sulfate
Active Ingredient(s): 15    mg/1 & nbsp;   Morphine Sulfate
Administration Route(s): ORAL; ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Morphine Sulfate

Product NDC: 49999-845
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075295
Marketing Category: ANDA
Start Marketing Date: 20100917

Package Information of Morphine Sulfate

Package NDC: 49999-845-60
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49999-845-60)

NDC Information of Morphine Sulfate

NDC Code 49999-845-60
Proprietary Name Morphine Sulfate
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49999-845-60)
Product NDC 49999-845
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Morphine Sulfate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL; ORAL
Start Marketing Date 20100917
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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