Pleo Rub - 60681-3301-1 - (aspergillus ruber)

Alphabetical Index


Drug Information of Pleo Rub

Product NDC: 60681-3301
Proprietary Name: Pleo Rub
Non Proprietary Name: aspergillus ruber
Active Ingredient(s): 5    [hp_X]/10mL & nbsp;   aspergillus ruber
Administration Route(s): ORAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Pleo Rub

Product NDC: 60681-3301
Labeler Name: Sanum Kehlbeck GmbH & Co. KG
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19960319

Package Information of Pleo Rub

Package NDC: 60681-3301-1
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (60681-3301-1) > 10 mL in 1 BOTTLE, DROPPER

NDC Information of Pleo Rub

NDC Code 60681-3301-1
Proprietary Name Pleo Rub
Package Description 1 BOTTLE, DROPPER in 1 CARTON (60681-3301-1) > 10 mL in 1 BOTTLE, DROPPER
Product NDC 60681-3301
Product Type Name HUMAN OTC DRUG
Non Proprietary Name aspergillus ruber
Dosage Form Name SOLUTION/ DROPS
Route Name ORAL
Start Marketing Date 19960319
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Sanum Kehlbeck GmbH & Co. KG
Substance Name ASPERGILLUS RUBER
Strength Number 5
Strength Unit [hp_X]/10mL
Pharmaceutical Classes

Complete Information of Pleo Rub


General Information