Product NDC: | 57520-0398 |
Proprietary Name: | Zyvestra |
Non Proprietary Name: | Cocculus indicus, Ferrum metallicum, Gelsemium sempervirens, Phytolacca decandra, Pulsatilla, Silicea, |
Active Ingredient(s): | 55; 55; 55; 55; 55 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; Cocculus indicus, Ferrum metallicum, Gelsemium sempervirens, Phytolacca decandra, Pulsatilla, Silicea, |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57520-0398 |
Labeler Name: | Apotheca Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20101203 |
Package NDC: | 57520-0398-1 |
Package Description: | 60 TABLET in 1 BOTTLE (57520-0398-1) |
NDC Code | 57520-0398-1 |
Proprietary Name | Zyvestra |
Package Description | 60 TABLET in 1 BOTTLE (57520-0398-1) |
Product NDC | 57520-0398 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Cocculus indicus, Ferrum metallicum, Gelsemium sempervirens, Phytolacca decandra, Pulsatilla, Silicea, |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20101203 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Apotheca Company |
Substance Name | ANAMIRTA COCCULUS SEED; GELSEMIUM SEMPERVIRENS ROOT; IRON; PHYTOLACCA AMERICANA ROOT; SILICON DIOXIDE |
Strength Number | 55; 55; 55; 55; 55 |
Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
Pharmaceutical Classes |