Sodium Chloride

Product NDC

0264-9999

11-digit product format

002649999

Labeler code

0264

Product ID

0264-9999_0b437b15-62f3-46e3-b4e2-89fa95143c23

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sodium Chloride

Dosage form

INJECTION

Route

INTRAVENOUS

Labeler

B. Braun Medical Inc.

Marketing category

UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE

Marketing start

2017-12-22

Marketing end

0000-00-00

Substance

SODIUM CHLORIDE

Active strength

900 mg/1000mL

Pharmacologic classes

Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record