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Pleo Cerivi
Pleo Cerivi - 60681-7002-1 - (Cetraria islandica subsp. islandica)
Drug Information of Pleo Cerivi
| Product NDC: | 60681-7002 |
| Proprietary Name: | Pleo Cerivi |
| Non Proprietary Name: | Cetraria islandica subsp. islandica |
| Active Ingredient(s): | 3 [hp_X]/2mL & nbsp; Cetraria islandica subsp. islandica |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pleo Cerivi
| Product NDC: | 60681-7002 |
| 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 Cerivi
| Package NDC: | 60681-7002-1 |
| Package Description: | 10 VIAL, GLASS in 1 CARTON (60681-7002-1) > 1 mL in 1 VIAL, GLASS |
NDC Information of Pleo Cerivi
| NDC Code | 60681-7002-1 |
| Proprietary Name | Pleo Cerivi |
| Package Description | 10 VIAL, GLASS in 1 CARTON (60681-7002-1) > 1 mL in 1 VIAL, GLASS |
| Product NDC | 60681-7002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetraria islandica subsp. islandica |
| 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 | CETRARIA ISLANDICA SUBSP. ISLANDICA |
| Strength Number | 3 |
| Strength Unit | [hp_X]/2mL |
| Pharmaceutical Classes |
