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Morphine Sulfate - 0574-7116-12 - (MORPHINE SULFATE)

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Drug Information of Morphine Sulfate

Product NDC: 0574-7116
Proprietary Name: Morphine Sulfate
Non Proprietary Name: MORPHINE SULFATE
Active Ingredient(s): 30    mg/1 & nbsp;   MORPHINE SULFATE
Administration Route(s): RECTAL
Dosage Form(s): SUPPOSITORY
Coding System: National Drug Codes(NDC)

Labeler Information of Morphine Sulfate

Product NDC: 0574-7116
Labeler Name: Paddock Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19900901

Package Information of Morphine Sulfate

Package NDC: 0574-7116-12
Package Description: 12 PACKET in 1 BOX (0574-7116-12) > 1 SUPPOSITORY in 1 PACKET

NDC Information of Morphine Sulfate

NDC Code 0574-7116-12
Proprietary Name Morphine Sulfate
Package Description 12 PACKET in 1 BOX (0574-7116-12) > 1 SUPPOSITORY in 1 PACKET
Product NDC 0574-7116
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MORPHINE SULFATE
Dosage Form Name SUPPOSITORY
Route Name RECTAL
Start Marketing Date 19900901
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Paddock Laboratories, LLC
Substance Name MORPHINE SULFATE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Morphine Sulfate


General Information