Dextrose

Product NDC

0338-6346

11-digit product format

003386346

Labeler code

0338

Product ID

0338-6346_94832611-25b1-47e7-b3f3-509a8e17db5b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Dextrose monohydrate

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Baxter Healthcare Corporation

Application

NDA016673

Marketing category

NDA

Marketing start

1971-03-04

Marketing end

2020-06-30

Substance

DEXTROSE MONOHYDRATE

Active strength

50 g/1000mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record