Venapro - 50845-0002-1 - (Venapro)

Alphabetical Index


Drug Information of Venapro

Product NDC: 50845-0002
Proprietary Name: Venapro
Non Proprietary Name: Venapro
Active Ingredient(s): 3; 10; 3; 1; 1; 6; 3; 1    [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp;   Venapro
Administration Route(s): ORAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Venapro

Product NDC: 50845-0002
Labeler Name: Liddell Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100512

Package Information of Venapro

Package NDC: 50845-0002-1
Package Description: 30 mL in 1 BOTTLE, SPRAY (50845-0002-1)

NDC Information of Venapro

NDC Code 50845-0002-1
Proprietary Name Venapro
Package Description 30 mL in 1 BOTTLE, SPRAY (50845-0002-1)
Product NDC 50845-0002
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Venapro
Dosage Form Name SPRAY
Route Name ORAL
Start Marketing Date 20100512
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Liddell Laboratories, Inc.
Substance Name ARNICA MONTANA; CALCIUM FLUORIDE; COLLINSONIA CANADENSIS ROOT; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HORSE CHESTNUT; HYDROCHLORIC ACID; KRAMERIA LAPPACEA ROOT; SILYBUM MARIANUM SEED
Strength Number 3; 10; 3; 1; 1; 6; 3; 1
Strength Unit [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmaceutical Classes

Complete Information of Venapro


General Information