Dextrose

Product NDC: 0409-7918
11-digit product format: 004097918
Labeler code: 0409
Product ID: 0409-7918_f22bcda2-771d-4ac9-b69b-f8fe36205568
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: dextrose
Dosage form: INJECTION, SOLUTION
Route: INTRAVENOUS
Labeler: Hospira, Inc.
Application: NDA018561
Marketing category: NDA
Marketing start: 2005-07-14
Marketing end: 2021-08-01
Substance: DEXTROSE MONOHYDRATE
Active strength: 70 g/100mL
NDC exclude flag: No
Listing certified through: 0000-00-00
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0409-7918-19	2020-09-03	C162847	48780-1	ab0e2407-2be4-f274-e053-dbdaa90a6471	155f0dfd-657a-4fc4-11a7-5b84cc216c4c
0409-7918-19	2020-07-22	C162847	48780-1	ab0e2407-2be4-f274-e053-dbdaa90a6471	155f0dfd-657a-4fc4-11a7-5b84cc216c4c

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0409-7918-19	ML - Milliliter	0409-7918	fce93cc6-da60-48ad-95b1-472b61767ce1	1	2013-02-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0409-7918-19	00409791819	12 POUCH in 1 CASE (0409-7918-19) > 1 BAG in 1 POUCH > 500 mL in 1 BAG	12 pouch	2005-07-14	2021-08-01	No	No	Current