H. Pylori - 43742-0036-1 - (Helicobacter pylori,)

Alphabetical Index


Drug Information of H. Pylori

Product NDC: 43742-0036
Proprietary Name: H. Pylori
Non Proprietary Name: Helicobacter pylori,
Active Ingredient(s): 15    [hp_X]/mL & nbsp;   Helicobacter pylori,
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of H. Pylori

Product NDC: 43742-0036
Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20120517

Package Information of H. Pylori

Package NDC: 43742-0036-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (43742-0036-1)

NDC Information of H. Pylori

NDC Code 43742-0036-1
Proprietary Name H. Pylori
Package Description 30 mL in 1 BOTTLE, DROPPER (43742-0036-1)
Product NDC 43742-0036
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Helicobacter pylori,
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20120517
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Deseret Biologicals, Inc.
Substance Name HELICOBACTER PYLORI
Strength Number 15
Strength Unit [hp_X]/mL
Pharmaceutical Classes

Complete Information of H. Pylori


General Information