Label: KANAPLEX- kanamycin a sulfate powder
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NDC Code(s):
55999-089-12,
55999-089-15,
55999-089-18,
55999-089-56, view more55999-089-57
- Packager: Seachem Laboratories Inc.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated July 13, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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VETERINARY INDICATIONS
KanaPlex™ is a blended kanamycin based medication that safely and effectively treats several fungal, and bacterial fish diseases (dropsy, popeye, fin/tail rot, septicemia). Because it is absorbed by fish it is useful in treating internal infections in those situations where food is refused. It does not adversely affect the filter bed and is easily removed with carbon.
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DOSAGE & ADMINISTRATION
DIRECTIONS: Use 1 level measure (included) to every 20 L (5 gallons). Repeat every 2 days until symptoms disappear or up to a maximum of 3 doses. Turn off UV, ozone, and chemical filtration. To feed, blend 1 measure with about 1 tablespoon of frozen food paste. To minimize loss during feeding use with Focus™. To enhance palatability use with GarlicGuard™ or Entice™. Food may be refrozen.
- SPL UNCLASSIFIED SECTION
- SAFE HANDLING WARNING
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 5 g Vial Carton
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INGREDIENTS AND APPEARANCE
KANAPLEX
kanamycin a sulfate powderProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:55999-089 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength KANAMYCIN A SULFATE (UNII: J80EX28SMQ) (Kanamycin A - UNII:EQK9Q303C5) Kanamycin A 317 mg in 1 g Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55999-089-56 6 in 1 CASE 1 NDC:55999-089-57 1 in 1 CARTON 1 NDC:55999-089-12 5 g in 1 VIAL, PLASTIC 2 NDC:55999-089-15 100 g in 1 VIAL, PLASTIC 3 NDC:55999-089-18 1000 g in 1 VIAL, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED DRUG OTHER 01/01/1999 Labeler - Seachem Laboratories Inc. (133041806)
