Sodium Chloride

Product NDC

55154-6979

11-digit product format

551546979

Labeler code

55154

Product ID

55154-6979_8d0189e7-b00f-4bd4-b532-64d132f02514

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sodium Chloride

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS

Labeler

Cardinal Health

Application

NDA018803

Marketing category

NDA

Marketing start

2011-09-08

Marketing end

0000-00-00

Substance

SODIUM CHLORIDE

Active strength

9 mg/mL

Pharmacologic classes

Osmotic Laxativ

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record