NDC 13985-808 - Sterile Water

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 13985-808
Package NDCs from labels: 13985-808-25, 13985-808-50, 13985-808-60
Manufacturer: MWI (VetOne) | Nova-Tech, Inc.
Effective date: 2014-06-10
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Sterile Water For Injection USP	MWI (VetOne) \| Nova-Tech, Inc.	2014-06-10	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
13985-808-25	Sterile Water	250 mL in 1 BOTTLE, PLASTIC	INJECTION	250	1
13985-808-50	Sterile Water	500 mL in 1 BOTTLE, PLASTIC	INJECTION	500	1
13985-808-60	Sterile Water	1000 mL in 1 BOTTLE, PLASTIC	INJECTION	1000	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
13985-808	STERILE WATER INJECTION [MWI (VETONE)]	1	3 package rows	20140611_2eeb04ab-52bd-4338-856a-4a7bfce3fbff.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
WATER	ACTIVE INGREDIENT	059QF0KO0R	STERILE WATER INJECTION [MWI (VETONE)]	1
WATER	ACTIVE MOIETY	059QF0KO0R	STERILE WATER INJECTION [MWI (VETONE)]	1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 9 of 9 · 161 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.