Dextrose

Product NDC

70518-1427

11-digit product format

705181427

Labeler code

70518

Product ID

70518-1427_7655e699-c7b1-607e-e053-2991aa0aaf24

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

DEXTROSE MONOHYDRATE

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

REMEDYREPACK INC.

Application

NDA019445

Marketing category

NDA

Marketing start

2018-09-18

Marketing end

0000-00-00

Substance

DEXTROSE MONOHYDRATE

Active strength

25 g/50mL

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record