Home
>
National Drug Code (NDC)
>
Pulsatilla
Pulsatilla - 57520-0629-1 - (Pulsatilla,)
Drug Information of Pulsatilla
| Product NDC: | 57520-0629 |
| Proprietary Name: | Pulsatilla |
| Non Proprietary Name: | Pulsatilla, |
| Active Ingredient(s): | 12 [hp_X]/g & nbsp; Pulsatilla, |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pulsatilla
| Product NDC: | 57520-0629 |
| Labeler Name: | Apotheca Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20110623 |
Package Information of Pulsatilla
| Package NDC: | 57520-0629-1 |
| Package Description: | 15 g in 1 BOTTLE (57520-0629-1) |
NDC Information of Pulsatilla
| NDC Code | 57520-0629-1 |
| Proprietary Name | Pulsatilla |
| Package Description | 15 g in 1 BOTTLE (57520-0629-1) |
| Product NDC | 57520-0629 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pulsatilla, |
| Dosage Form Name | PELLET |
| Route Name | ORAL |
| Start Marketing Date | 20110623 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Apotheca Company |
| Substance Name | PULSATILLA VULGARIS |
| Strength Number | 12 |
| Strength Unit | [hp_X]/g |
| Pharmaceutical Classes |
