Calcium Acetate

Product NDC

0574-0113

11-digit product format

005740113

Labeler code

0574

Product ID

0574-0113_2b9a0eb8-4781-4930-b623-501e2000d068

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

CALCIUM ACETATE

Dosage form

TABLET

Route

ORAL

Labeler

Paddock Laboratories, LLC

Application

ANDA091561

Marketing category

ANDA

Marketing start

2011-09-13

Marketing end

2020-10-31

Substance

CALCIUM ACETATE

Active strength

667 mg/1

Pharmacologic classes

Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record