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Venapro
Venapro - 50845-0002-1 - (Venapro)
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 |
