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Bryonia Alba
Bryonia Alba - 57471-3061-3 - (Bryonia Alba)
Drug Information of Bryonia Alba
| Product NDC: | 57471-3061 |
| Proprietary Name: | Bryonia Alba |
| Non Proprietary Name: | Bryonia Alba |
| Active Ingredient(s): | 30 [hp_C]/1 & nbsp; Bryonia Alba |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bryonia Alba
| Product NDC: | 57471-3061 |
| Labeler Name: | Celletech Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19880701 |
Package Information of Bryonia Alba
| Package NDC: | 57471-3061-3 |
| Package Description: | 800 PELLET in 1 BOTTLE (57471-3061-3) |
NDC Information of Bryonia Alba
| NDC Code | 57471-3061-3 |
| Proprietary Name | Bryonia Alba |
| Package Description | 800 PELLET in 1 BOTTLE (57471-3061-3) |
| Product NDC | 57471-3061 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bryonia Alba |
| Dosage Form Name | PELLET |
| Route Name | ORAL |
| Start Marketing Date | 19880701 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Celletech Ltd. |
| Substance Name | BRYONIA ALBA ROOT |
| Strength Number | 30 |
| Strength Unit | [hp_C]/1 |
| Pharmaceutical Classes |
