ELIPHOS - 0179-0098-70 - (Calcium Acetate)

Alphabetical Index


Drug Information of ELIPHOS

Product NDC: 0179-0098
Proprietary Name: ELIPHOS
Non Proprietary Name: Calcium Acetate
Active Ingredient(s): 667    mg/1 & nbsp;   Calcium Acetate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ELIPHOS

Product NDC: 0179-0098
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078502
Marketing Category: ANDA
Start Marketing Date: 20110824

Package Information of ELIPHOS

Package NDC: 0179-0098-70
Package Description: 30 TABLET in 1 BOX, UNIT-DOSE (0179-0098-70)

NDC Information of ELIPHOS

NDC Code 0179-0098-70
Proprietary Name ELIPHOS
Package Description 30 TABLET in 1 BOX, UNIT-DOSE (0179-0098-70)
Product NDC 0179-0098
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Calcium Acetate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110824
Marketing Category Name ANDA
Labeler Name KAISER FOUNDATION HOSPITALS
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 ELIPHOS


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