Label: MANNITOL 20%- mannitol injection
- NDC Code(s): 13985-052-15
- Packager: MWI (VetOne)
- Category: PRESCRIPTION ANIMAL DRUG LABEL
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Drug Label Information
Updated May 13, 2024
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- INDICATIONS:
- Each 100 mL Contains:
- Dosage and Administration:
- Note:
- Storage:
- SPL UNCLASSIFIED SECTION
- WARNINGS AND PRECAUTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MANNITOL 20%
mannitol injectionProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:13985-052 Route of Administration INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MANNITOL (UNII: 3OWL53L36A) (MANNITOL - UNII:3OWL53L36A) MANNITOL 20 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:13985-052-15 100 mL in 1 VIAL, SINGLE-USE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/20/2011 Labeler - MWI (VetOne) (019926120)