Sodium Lactate

Product NDC

0409-6664

11-digit product format

004096664

Labeler code

0409

Product ID

0409-6664_37def875-6c99-449f-8883-2d4a8004f030

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

SODIUM LACTATE

Dosage form

INJECTION, SOLUTION, CONCENTRATE

Route

INTRAVENOUS

Labeler

Hospira, Inc.

Application

NDA018947

Marketing category

NDA

Marketing start

2006-06-28

Marketing end

0000-00-00

Substance

SODIUM LACTATE

Active strength

6 g/10mL

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record