SODIUM CHLORIDE

Product NDC

0338-9604

11-digit product format

003389604

Labeler code

0338

Product ID

0338-9604_dd447145-6de8-4f6b-8637-ebf8f5bc502e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

sodium chloride

Dosage form

INJECTION

Route

INTRAVENOUS

Labeler

Baxter Healthcare Corporation

Marketing category

UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE

Marketing start

2017-10-13

Marketing end

0000-00-00

Substance

SODIUM CHLORIDE

Active strength

900 mg/100mL

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

2020-12-31

Current FDA listing

Historical FDA.report record