Idoxuridine: Package Insert and Label Information

IDOXURIDINE- idoxuridine powder


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idoxuridine powder
Product Information
Product Type Item Code (Source) NDC:71052-140
Route of Administration NOT APPLICABLE DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Idoxuridine (IDOXURIDINE) Idoxuridine 1 kg in 1 kg
# Item Code Package Description Multilevel Packaging
1 NDC:71052-140-10 0.1 kg in 1 PACKAGE None
2 NDC:71052-140-25 0.025 kg in 1 PACKAGE None
3 NDC:71052-140-02 0.005 kg in 1 PACKAGE None
4 NDC:71052-140-01 0.001 kg in 1 PACKAGE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
bulk ingredient for animal drug compounding 01/25/2023
Labeler — DARMERICA, LLC (080233052)

Revised: 01/2023 DARMERICA, LLC provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

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