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Aconite
Aconite - 57520-0559-1 - (Aconitum napellus,)
Drug Information of Aconite
| Product NDC: | 57520-0559 |
| Proprietary Name: | Aconite |
| Non Proprietary Name: | Aconitum napellus, |
| Active Ingredient(s): | 12 [hp_X]/mL & nbsp; Aconitum napellus, |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aconite
| Product NDC: | 57520-0559 |
| Labeler Name: | Apotheca Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20100922 |
Package Information of Aconite
| Package NDC: | 57520-0559-1 |
| Package Description: | 15 mL in 1 BOTTLE (57520-0559-1) |
NDC Information of Aconite
| NDC Code | 57520-0559-1 |
| Proprietary Name | Aconite |
| Package Description | 15 mL in 1 BOTTLE (57520-0559-1) |
| Product NDC | 57520-0559 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aconitum napellus, |
| Dosage Form Name | PELLET |
| Route Name | ORAL |
| Start Marketing Date | 20100922 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Apotheca Company |
| Substance Name | ACONITUM NAPELLUS |
| Strength Number | 12 |
| Strength Unit | [hp_X]/mL |
| Pharmaceutical Classes |
