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Pleo Oku
Pleo Oku - 60681-2402-2 - (OKOUBAKA AUBREVILLEI BARK)
Drug Information of Pleo Oku
| Product NDC: | 60681-2402 |
| Proprietary Name: | Pleo Oku |
| Non Proprietary Name: | OKOUBAKA AUBREVILLEI BARK |
| Active Ingredient(s): | 2 [hp_X]/1 & nbsp; OKOUBAKA AUBREVILLEI BARK |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pleo Oku
| Product NDC: | 60681-2402 |
| Labeler Name: | Sanum-Kehlbeck GmbH & Co. KG |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20120710 |
Package Information of Pleo Oku
| Package NDC: | 60681-2402-2 |
| Package Description: | 8 BLISTER PACK in 1 CARTON (60681-2402-2) > 10 TABLET in 1 BLISTER PACK |
NDC Information of Pleo Oku
| NDC Code | 60681-2402-2 |
| Proprietary Name | Pleo Oku |
| Package Description | 8 BLISTER PACK in 1 CARTON (60681-2402-2) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 60681-2402 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OKOUBAKA AUBREVILLEI BARK |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120710 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Sanum-Kehlbeck GmbH & Co. KG |
| Substance Name | OKOUBAKA AUBREVILLEI BARK |
| Strength Number | 2 |
| Strength Unit | [hp_X]/1 |
| Pharmaceutical Classes |
