Product NDC: | 60681-5604 |
Proprietary Name: | Pleo Usti |
Non Proprietary Name: | ustilago maydis |
Active Ingredient(s): | 5 [HP_X]/1 & nbsp; ustilago maydis |
Administration Route(s): | RECTAL |
Dosage Form(s): | SUPPOSITORY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60681-5604 |
Labeler Name: | Sanum Kehlbeck GmbH & Co. KG |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20040421 |
Package NDC: | 60681-5604-1 |
Package Description: | 1 DOSE PACK in 1 CARTON (60681-5604-1) > 10 SUPPOSITORY in 1 DOSE PACK |
NDC Code | 60681-5604-1 |
Proprietary Name | Pleo Usti |
Package Description | 1 DOSE PACK in 1 CARTON (60681-5604-1) > 10 SUPPOSITORY in 1 DOSE PACK |
Product NDC | 60681-5604 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ustilago maydis |
Dosage Form Name | SUPPOSITORY |
Route Name | RECTAL |
Start Marketing Date | 20040421 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Sanum Kehlbeck GmbH & Co. KG |
Substance Name | USTILAGO MAYDIS |
Strength Number | 5 |
Strength Unit | [HP_X]/1 |
Pharmaceutical Classes |