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Morphinum Muriaticum - 10191-1029-2 - (Morphine Hydrochloride)

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Drug Information of Morphinum Muriaticum

Product NDC: 10191-1029
Proprietary Name: Morphinum Muriaticum
Non Proprietary Name: Morphine Hydrochloride
Active Ingredient(s): 30    [hp_C]/1 & nbsp;   Morphine Hydrochloride
Administration Route(s): SUBLINGUAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of Morphinum Muriaticum

Product NDC: 10191-1029
Labeler Name: Remedy Makers
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20020409

Package Information of Morphinum Muriaticum

Package NDC: 10191-1029-2
Package Description: 130 PELLET in 1 VIAL, GLASS (10191-1029-2)

NDC Information of Morphinum Muriaticum

NDC Code 10191-1029-2
Proprietary Name Morphinum Muriaticum
Package Description 130 PELLET in 1 VIAL, GLASS (10191-1029-2)
Product NDC 10191-1029
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Morphine Hydrochloride
Dosage Form Name PELLET
Route Name SUBLINGUAL
Start Marketing Date 20020409
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Remedy Makers
Substance Name MORPHINE HYDROCHLORIDE
Strength Number 30
Strength Unit [hp_C]/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Morphinum Muriaticum


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