Product NDC: | 0220-3681 |
Proprietary Name: | Nux Vomica |
Non Proprietary Name: | STRYCHNOS NUX-VOMICA SEED |
Active Ingredient(s): | 30 [hp_C]/1 & nbsp; STRYCHNOS NUX-VOMICA SEED |
Administration Route(s): | ORAL |
Dosage Form(s): | PELLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0220-3681 |
Labeler Name: | Laboratoires Boiron |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20120101 |
Package NDC: | 0220-3681-43 |
Package Description: | 3 TUBE in 1 PACKAGE (0220-3681-43) > 80 PELLET in 1 TUBE (0220-3681-41) |
NDC Code | 0220-3681-43 |
Proprietary Name | Nux Vomica |
Package Description | 3 TUBE in 1 PACKAGE (0220-3681-43) > 80 PELLET in 1 TUBE (0220-3681-41) |
Product NDC | 0220-3681 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | STRYCHNOS NUX-VOMICA SEED |
Dosage Form Name | PELLET |
Route Name | ORAL |
Start Marketing Date | 20120101 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Laboratoires Boiron |
Substance Name | STRYCHNOS NUX-VOMICA SEED |
Strength Number | 30 |
Strength Unit | [hp_C]/1 |
Pharmaceutical Classes |