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Pleo Ex
Pleo Ex - 60681-1005-2 - (candida albicans, candida parapsilosis and penicillium roqueforti)
Drug Information of Pleo Ex
| Product NDC: | 60681-1005 |
| Proprietary Name: | Pleo Ex |
| Non Proprietary Name: | candida albicans, candida parapsilosis and penicillium roqueforti |
| Active Ingredient(s): | 5; 5; 5 [HP_X]/mL; [HP_X]/mL; [HP_X]/mL & nbsp; candida albicans, candida parapsilosis and penicillium roqueforti |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pleo Ex
| Product NDC: | 60681-1005 |
| Labeler Name: | Sanum Kehlbeck GmbH & Co. KG |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19980119 |
Package Information of Pleo Ex
| Package NDC: | 60681-1005-2 |
| Package Description: | 50 VIAL, GLASS in 1 CARTON (60681-1005-2) > 1 mL in 1 VIAL, GLASS |
NDC Information of Pleo Ex
| NDC Code | 60681-1005-2 |
| Proprietary Name | Pleo Ex |
| Package Description | 50 VIAL, GLASS in 1 CARTON (60681-1005-2) > 1 mL in 1 VIAL, GLASS |
| Product NDC | 60681-1005 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | candida albicans, candida parapsilosis and penicillium roqueforti |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19980119 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Sanum Kehlbeck GmbH & Co. KG |
| Substance Name | CANDIDA ALBICANS; CANDIDA PARAPSILOSIS; PENICILLIUM ROQUEFORTI |
| Strength Number | 5; 5; 5 |
| Strength Unit | [HP_X]/mL; [HP_X]/mL; [HP_X]/mL |
| Pharmaceutical Classes |
