Label: MANNITOL 20%- mannitol injection
- NDC Code(s): 59051-8061-5
- Packager: Neogen Corporation
- Category: PRESCRIPTION ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 22, 2019
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- INDICATIONS:
- Each 100 mL Contains:
- Dosage and Administration:
- Note:
- STORAGE AND HANDLING
-
SPL UNCLASSIFIED SECTION
RMS 92-384
Made in the USA
Item No. 09061
NDC 59051-8061-5
Mannitol Injection 20%
Sterile Solution
NeogenVet
Net Contentes: 100 mL
Lot No.
Exp. Date:
Neogen
Manufactured by: Nova-Tech, Grand Island, NE 68801
Manufactured for: Neogen Corporation, Lexington, KY 40511
859-254-1221
animalsafety.neogen.com
L566-0518
- WARNINGS AND PRECAUTIONS
- Mannitol Injection 20%
-
INGREDIENTS AND APPEARANCE
MANNITOL 20%
mannitol injectionProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:59051-8061 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:59051-8061-5 100 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 - Neogen Corporation (042125879) Registrant - Nova-Tech, Inc (196078976) Establishment Name Address ID/FEI Business Operations Nova-Tech, Inc 196078976 manufacture