Home
>
National Drug Code (NDC)
>
Bio Holly
Bio Holly - 57520-0517-1 - (Holly,)
Drug Information of Bio Holly
| Product NDC: | 57520-0517 |
| Proprietary Name: | Bio Holly |
| Non Proprietary Name: | Holly, |
| Active Ingredient(s): | 200 [hp_C]/mL & nbsp; Holly, |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bio Holly
| Product NDC: | 57520-0517 |
| Labeler Name: | Apotheca Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20100616 |
Package Information of Bio Holly
| Package NDC: | 57520-0517-1 |
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (57520-0517-1) |
NDC Information of Bio Holly
| NDC Code | 57520-0517-1 |
| Proprietary Name | Bio Holly |
| Package Description | 30 mL in 1 BOTTLE, DROPPER (57520-0517-1) |
| Product NDC | 57520-0517 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Holly, |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20100616 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Apotheca Company |
| Substance Name | ILEX AQUIFOLIUM FLOWERING TOP |
| Strength Number | 200 |
| Strength Unit | [hp_C]/mL |
| Pharmaceutical Classes |
