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CANTHARIS
CANTHARIS - 60512-9151-1 - (CANTHARIS)
Drug Information of CANTHARIS
| Product NDC: | 60512-9151 |
| Proprietary Name: | CANTHARIS |
| Non Proprietary Name: | CANTHARIS |
| Active Ingredient(s): | 3 [hp_X]/1 & nbsp; CANTHARIS |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CANTHARIS
| Product NDC: | 60512-9151 |
| Labeler Name: | HOMEOLAB USA INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20111130 |
Package Information of CANTHARIS
| Package NDC: | 60512-9151-1 |
| Package Description: | 80 PELLET in 1 TUBE (60512-9151-1) |
NDC Information of CANTHARIS
| NDC Code | 60512-9151-1 |
| Proprietary Name | CANTHARIS |
| Package Description | 80 PELLET in 1 TUBE (60512-9151-1) |
| Product NDC | 60512-9151 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CANTHARIS |
| Dosage Form Name | PELLET |
| Route Name | ORAL |
| Start Marketing Date | 20111130 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | HOMEOLAB USA INC |
| Substance Name | LYTTA VESICATORIA |
| Strength Number | 3 |
| Strength Unit | [hp_X]/1 |
| Pharmaceutical Classes |
