Sodium Chloride

Product NDC

70518-1425

11-digit product format

705181425

Labeler code

70518

Product ID

70518-1425_76305882-6fda-33a0-e053-2991aa0ad5a2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

SODIUM CHLORIDE

Dosage form

INJECTION

Route

INTRAVENOUS

Labeler

REMEDYREPACK INC.

Application

ANDA088912

Marketing category

ANDA

Marketing start

2018-09-18

Marketing end

0000-00-00

Substance

SODIUM CHLORIDE

Active strength

9 mg/mL

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