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Thuja
Thuja - 53645-1220-2 - (Thuja)
Drug Information of Thuja
| Product NDC: | 53645-1220 |
| Proprietary Name: | Thuja |
| Non Proprietary Name: | Thuja |
| Active Ingredient(s): | 6 [hp_X]/23g & nbsp; Thuja |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GLOBULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Thuja
| Product NDC: | 53645-1220 |
| Labeler Name: | True Botanica, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20130621 |
Package Information of Thuja
| Package NDC: | 53645-1220-2 |
| Package Description: | 23 g in 1 BOTTLE (53645-1220-2) |
NDC Information of Thuja
| NDC Code | 53645-1220-2 |
| Proprietary Name | Thuja |
| Package Description | 23 g in 1 BOTTLE (53645-1220-2) |
| Product NDC | 53645-1220 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Thuja |
| Dosage Form Name | GLOBULE |
| Route Name | ORAL |
| Start Marketing Date | 20130621 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | True Botanica, LLC |
| Substance Name | THUJA OCCIDENTALIS LEAFY TWIG |
| Strength Number | 6 |
| Strength Unit | [hp_X]/23g |
| Pharmaceutical Classes |
