DEXTROSE

Product NDC

55154-2887

11-digit product format

551542887

Labeler code

55154

Product ID

55154-2887_4bdd5269-ed2c-47cb-b2ae-e7f2053480fa

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

DEXTROSE MONOHYDRATE

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Cardinal Health

Application

NDA016673

Marketing category

NDA

Marketing start

1971-03-04

Marketing end

0000-00-00

Substance

DEXTROSE MONOHYDRATE

Active strength

50 g/1000mL

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record