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Calcium Acetate - 0781-2672-02 - (Calcium Acetate)

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Drug Information of Calcium Acetate

Product NDC: 0781-2672
Proprietary Name: Calcium Acetate
Non Proprietary Name: Calcium Acetate
Active Ingredient(s): 667    mg/1 & nbsp;   Calcium Acetate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Calcium Acetate

Product NDC: 0781-2672
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021160
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20120314

Package Information of Calcium Acetate

Package NDC: 0781-2672-02
Package Description: 200 CAPSULE in 1 BOTTLE (0781-2672-02)

NDC Information of Calcium Acetate

NDC Code 0781-2672-02
Proprietary Name Calcium Acetate
Package Description 200 CAPSULE in 1 BOTTLE (0781-2672-02)
Product NDC 0781-2672
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Calcium Acetate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120314
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Sandoz Inc
Substance Name CALCIUM ACETATE
Strength Number 667
Strength Unit mg/1
Pharmaceutical Classes Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient]

Complete Information of Calcium Acetate


General Information