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morphine sulfate - 60951-659-70 - (morphine sulfate)

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Drug Information of morphine sulfate

Product NDC: 60951-659
Proprietary Name: morphine sulfate
Non Proprietary Name: morphine sulfate
Active Ingredient(s): 200    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: 60951-659
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075295
Marketing Category: ANDA
Start Marketing Date: 19981031

Package Information of morphine sulfate

Package NDC: 60951-659-70
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (60951-659-70)

NDC Information of morphine sulfate

NDC Code 60951-659-70
Proprietary Name morphine sulfate
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (60951-659-70)
Product NDC 60951-659
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name morphine sulfate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19981031
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
Substance Name MORPHINE SULFATE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of morphine sulfate


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