Label: RENAPLUS- potassium gluconate powder
- NDC Code(s): 13985-591-51
- Packager: MWI/VetOne
- Category: PRESCRIPTION ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated December 29, 2020
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- USE IN SPECIFIC POPULATIONS
- CONTAINS:
- DOSAGE:
- PRECAUTION:
- SPL UNCLASSIFIED SECTION
- WARNING:
- INDICATION:
- STORAGE:
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 4 oz Bottle
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INGREDIENTS AND APPEARANCE
RENAPLUS
potassium gluconate powderProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:13985-591 Route of Administration Oral Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM GLUCONATE (UNII: 12H3K5QKN9) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM GLUCONATE 468 mg in 0.65 g Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color brown Score Shape Size Flavor LIVER Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:13985-591-51 113 g in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/06/2014 Labeler - MWI/VetOne (019926120) Establishment Name Address ID/FEI Business Operations Neogen Corporation-Mercer 042125879 analysis, manufacture, label Establishment Name Address ID/FEI Business Operations Jungbunzlauer Ladenburg GmbH 322121609 api manufacture