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Calcium Acetate - 55154-4961-4 - (Calcium Acetate)

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Drug Information of Calcium Acetate

Product NDC: 55154-4961
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: 55154-4961
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077728
Marketing Category: ANDA
Start Marketing Date: 20080226

Package Information of Calcium Acetate

Package NDC: 55154-4961-4
Package Description: 200 POUCH in 1 CARTON (55154-4961-4) > 1 CAPSULE in 1 POUCH (55154-4961-6)

NDC Information of Calcium Acetate

NDC Code 55154-4961-4
Proprietary Name Calcium Acetate
Package Description 200 POUCH in 1 CARTON (55154-4961-4) > 1 CAPSULE in 1 POUCH (55154-4961-6)
Product NDC 55154-4961
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Calcium Acetate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20080226
Marketing Category Name ANDA
Labeler Name Cardinal Health
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


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