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Pleo Cerivi - 60681-7002-2 - (Cetraria islandica subsp. islandica)

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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: 60681-7002-2
Package Description: 50 VIAL, GLASS in 1 CARTON (60681-7002-2) > 1 mL in 1 VIAL, GLASS

NDC Information of Pleo Cerivi

NDC Code 60681-7002-2
Proprietary Name Pleo Cerivi
Package Description 50 VIAL, GLASS in 1 CARTON (60681-7002-2) > 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

Complete Information of Pleo Cerivi


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