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Morphine Sulfate - 49884-665-11 - (Morphine Sulfate)

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Drug Information of Morphine Sulfate

Product NDC: 49884-665
Proprietary Name: Morphine Sulfate
Non Proprietary Name: Morphine Sulfate
Active Ingredient(s): 20    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: 49884-665
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200812
Marketing Category: ANDA
Start Marketing Date: 20111110

Package Information of Morphine Sulfate

Package NDC: 49884-665-11
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49884-665-11)

NDC Information of Morphine Sulfate

NDC Code 49884-665-11
Proprietary Name Morphine Sulfate
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49884-665-11)
Product NDC 49884-665
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Morphine Sulfate
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20111110
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Inc.
Substance Name MORPHINE SULFATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Morphine Sulfate


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