Label: NEOPLEX- neomycin sulfate powder
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NDC Code(s):
55999-069-13,
55999-069-15,
55999-069-18,
55999-069-56, view more55999-069-57
- Packager: Seachem Laboratories Inc.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated July 16, 2018
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- Official Label (Printer Friendly)
- VETERINARY INDICATIONS
- DOSAGE & ADMINISTRATION
- SPL UNCLASSIFIED SECTION
- SAFE HANDLING WARNING
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 10 g Vial Carton
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INGREDIENTS AND APPEARANCE
NEOPLEX
neomycin sulfate powderProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:55999-069 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Neomycin Sulfate (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) Neomycin Sulfate 425 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:55999-069-56 6 in 1 CASE 1 NDC:55999-069-57 1 in 1 CARTON 1 NDC:55999-069-13 10 g in 1 VIAL, PLASTIC 2 NDC:55999-069-15 100 g in 1 VIAL, PLASTIC 3 NDC:55999-069-18 1000 g in 1 VIAL, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved drug other 01/01/1985 Labeler - Seachem Laboratories Inc. (133041806)