Calcium Acetate (Page 3 of 3)

PRINCIPAL DISPLAY PANEL — NDC: 0781-2081-02

Calcium Acetate -- Bottle Label 200 Capsules
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — NDC: 0781-2672-02

Calcium acetate figure 3
(click image for full-size original)

CALCIUM ACETATE
calcium acetate capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0781-2081
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CALCIUM ACETATE (CALCIUM CATION) CALCIUM ACETATE 667 mg
Product Characteristics
Color white, blue Score no score
Shape CAPSULE Size 21mm
Flavor Imprint Code SANDOZ;576
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0781-2081-02 200 CAPSULE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA authorized generic NDA021160 03/14/2012 03/31/2024
CALCIUM ACETATE
calcium acetate capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0781-2672
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CALCIUM ACETATE (CALCIUM CATION) CALCIUM ACETATE 667 mg
Product Characteristics
Color white, blue Score no score
Shape CAPSULE Size 21mm
Flavor Imprint Code SANDOZ;576
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0781-2672-02 200 CAPSULE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA authorized generic NDA021160 03/14/2012 03/31/2024
Labeler — Sandoz Inc (005387188)
Registrant — Fresenius Medical Care North America (958291411)

Revised: 10/2023 Sandoz Inc

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