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Opium Tincture (Deodorized) - 42998-203-01 - (Morphine (anhydrous))

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Drug Information of Opium Tincture (Deodorized)

Product NDC: 42998-203
Proprietary Name: Opium Tincture (Deodorized)
Non Proprietary Name: Morphine (anhydrous)
Active Ingredient(s): 10    mg/mL & nbsp;   Morphine (anhydrous)
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Opium Tincture (Deodorized)

Product NDC: 42998-203
Labeler Name: Marathon Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20080925

Package Information of Opium Tincture (Deodorized)

Package NDC: 42998-203-01
Package Description: 118 mL in 1 BOTTLE, GLASS (42998-203-01)

NDC Information of Opium Tincture (Deodorized)

NDC Code 42998-203-01
Proprietary Name Opium Tincture (Deodorized)
Package Description 118 mL in 1 BOTTLE, GLASS (42998-203-01)
Product NDC 42998-203
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Morphine (anhydrous)
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20080925
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Marathon Pharmaceuticals, LLC
Substance Name MORPHINE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Opium Tincture (Deodorized)


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