Sodium Chloride

Product NDC

0409-7730

11-digit product format

004097730

Labeler code

0409

Product ID

0409-7730_9788db74-ff4f-41d6-9c2e-f8d4850e5662

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

SODIUM CHLORIDE

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Hospira, Inc.

Application

NDA018090

Marketing category

NDA

Marketing start

1979-04-04

Marketing end

2020-08-01

Substance

SODIUM CHLORIDE

Active strength

450 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

0000-00-00

Current FDA listing

Historical FDA.report record