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Belladonna
Belladonna - 53645-1111-2 - (Belladonna)
Drug Information of Belladonna
| Product NDC: | 53645-1111 |
| Proprietary Name: | Belladonna |
| Non Proprietary Name: | Belladonna |
| Active Ingredient(s): | 6 [hp_X]/23g & nbsp; Belladonna |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GLOBULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Belladonna
| Product NDC: | 53645-1111 |
| Labeler Name: | True Botanica, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20130607 |
Package Information of Belladonna
| Package NDC: | 53645-1111-2 |
| Package Description: | 23 g in 1 BOTTLE (53645-1111-2) |
NDC Information of Belladonna
| NDC Code | 53645-1111-2 |
| Proprietary Name | Belladonna |
| Package Description | 23 g in 1 BOTTLE (53645-1111-2) |
| Product NDC | 53645-1111 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Belladonna |
| Dosage Form Name | GLOBULE |
| Route Name | ORAL |
| Start Marketing Date | 20130607 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | True Botanica, LLC |
| Substance Name | ATROPA BELLADONNA |
| Strength Number | 6 |
| Strength Unit | [hp_X]/23g |
| Pharmaceutical Classes |
