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Epstein-Barr Virus Remedy - 43742-0192-1 - (Epstein-Barr Virus)

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Drug Information of Epstein-Barr Virus Remedy

Product NDC: 43742-0192
Proprietary Name: Epstein-Barr Virus Remedy
Non Proprietary Name: Epstein-Barr Virus
Active Ingredient(s): 15    [hp_X]/mL & nbsp;   Epstein-Barr Virus
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Epstein-Barr Virus Remedy

Product NDC: 43742-0192
Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20121029

Package Information of Epstein-Barr Virus Remedy

Package NDC: 43742-0192-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (43742-0192-1)

NDC Information of Epstein-Barr Virus Remedy

NDC Code 43742-0192-1
Proprietary Name Epstein-Barr Virus Remedy
Package Description 30 mL in 1 BOTTLE, DROPPER (43742-0192-1)
Product NDC 43742-0192
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Epstein-Barr Virus
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20121029
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Deseret Biologicals, Inc.
Substance Name HUMAN HERPESVIRUS 4
Strength Number 15
Strength Unit [hp_X]/mL
Pharmaceutical Classes

Complete Information of Epstein-Barr Virus Remedy


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