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Pleo Usti
Pleo Usti - 60681-5601-1 - (ustilago maydis)
Drug Information of Pleo Usti
| Product NDC: | 60681-5601 |
| Proprietary Name: | Pleo Usti |
| Non Proprietary Name: | ustilago maydis |
| Active Ingredient(s): | 5 [hp_X]/10mL & nbsp; ustilago maydis |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pleo Usti
| Product NDC: | 60681-5601 |
| Labeler Name: | Sanum Kehlbeck GmbH & Co. KG |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19980819 |
Package Information of Pleo Usti
| Package NDC: | 60681-5601-1 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (60681-5601-1) > 30 mL in 1 BOTTLE, DROPPER |
NDC Information of Pleo Usti
| NDC Code | 60681-5601-1 |
| Proprietary Name | Pleo Usti |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (60681-5601-1) > 30 mL in 1 BOTTLE, DROPPER |
| Product NDC | 60681-5601 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ustilago maydis |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | ORAL |
| Start Marketing Date | 19980819 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Sanum Kehlbeck GmbH & Co. KG |
| Substance Name | USTILAGO MAYDIS |
| Strength Number | 5 |
| Strength Unit | [hp_X]/10mL |
| Pharmaceutical Classes |
