NDC 57520-0398
Zyvestra
Cocculus Indicus, Ferrum Metallicum, Gelsemium Sempervirens, Phytolacca Decandra, Pulsatilla, Silicea,
Zyvestra is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Apotheca Company. The primary component is Anamirta Cocculus Seed; Iron; Gelsemium Sempervirens Root; Phytolacca Americana Root; Silicon Dioxide.
| Product ID | 57520-0398_c3e70690-16e5-4dad-8f29-16b6a6f82e81 |
| NDC | 57520-0398 |
| Product Type | Human Otc Drug |
| Proprietary Name | Zyvestra |
| Generic Name | Cocculus Indicus, Ferrum Metallicum, Gelsemium Sempervirens, Phytolacca Decandra, Pulsatilla, Silicea, |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2010-12-03 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | Apotheca Company |
| Substance Name | ANAMIRTA COCCULUS SEED; IRON; GELSEMIUM SEMPERVIRENS ROOT; PHYTOLACCA AMERICANA ROOT; SILICON DIOXIDE |
| Active Ingredient Strength | 55 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
Packaging
NDC 57520-0398-1
60 TABLET in 1 BOTTLE (57520-0398-1)
| Marketing Start Date | 2010-12-03 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 57520-0398-1 [57520039801]
Zyvestra TABLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-12-03 |
| Inactivation Date | 2020-01-31 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| ANAMIRTA COCCULUS SEED | 55 [hp_X]/1 |
OpenFDA Data
| SPL SET ID: | b55d309e-40fc-4b9b-bbcc-361767e5ef0f |
| Manufacturer | |
| UNII |
Trademark Results [Zyvestra]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ZYVESTRA 85179158 3993111 Dead/Cancelled |
Selfworx.com LLC 2010-11-17 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.