Rubus - 60986-1011-3 - (Rubus Fruticosus, Iris Germanica, Vaccinium Myrtillus, Syzygium Jambolanum, Okoubaka Aubrevillei)

Alphabetical Index


Drug Information of Rubus

Product NDC: 60986-1011
Proprietary Name: Rubus
Non Proprietary Name: Rubus Fruticosus, Iris Germanica, Vaccinium Myrtillus, Syzygium Jambolanum, Okoubaka Aubrevillei
Active Ingredient(s): 3; 2; 4; 6; 3    [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL & nbsp;   Rubus Fruticosus, Iris Germanica, Vaccinium Myrtillus, Syzygium Jambolanum, Okoubaka Aubrevillei
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Rubus

Product NDC: 60986-1011
Labeler Name: Marco Pharma International LLC.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19920301

Package Information of Rubus

Package NDC: 60986-1011-3
Package Description: 50 mL in 1 BOTTLE, GLASS (60986-1011-3)

NDC Information of Rubus

NDC Code 60986-1011-3
Proprietary Name Rubus
Package Description 50 mL in 1 BOTTLE, GLASS (60986-1011-3)
Product NDC 60986-1011
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Rubus Fruticosus, Iris Germanica, Vaccinium Myrtillus, Syzygium Jambolanum, Okoubaka Aubrevillei
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19920301
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Marco Pharma International LLC.
Substance Name BILBERRY; BLACKBERRY; IRIS GERMANICA ROOT; OKOUBAKA AUBREVILLEI BARK; SYZYGIUM CUMINI SEED
Strength Number 3; 2; 4; 6; 3
Strength Unit [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL
Pharmaceutical Classes

Complete Information of Rubus


General Information