Calcium Gluconate

Product NDC

0517-3900

11-digit product format

005173900

Labeler code

0517

Product ID

0517-3900_5178d569-7ff6-46de-a8ce-498e9608ef3f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Calcium Gluconate

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

American Regent, Inc.

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

1992-12-01

Marketing end

0000-00-00

Substance

CALCIUM GLUCONATE MONOHYDRATE

Active strength

98 mg/mL

Pharmacologic classes

Calcium [CS],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record