Calcium Acetate

Product NDC

70518-2231

11-digit product format

705182231

Labeler code

70518

Product ID

70518-2231_8f53b42d-b656-f946-e053-2a95a90a7884

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Calcium Acetate

Dosage form

CAPSULE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA203179

Marketing category

ANDA

Marketing start

2019-07-23

Marketing end

0000-00-00

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

2020-12-31

Current FDA listing

Historical FDA.report record