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CALCIUM ACETATE - 49349-064-02 - (CALCIUM ACETATE)

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Drug Information of CALCIUM ACETATE

Product NDC: 49349-064
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: 49349-064
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077728
Marketing Category: ANDA
Start Marketing Date: 20101111

Package Information of CALCIUM ACETATE

Package NDC: 49349-064-02
Package Description: 30 CAPSULE in 1 BLISTER PACK (49349-064-02)

NDC Information of CALCIUM ACETATE

NDC Code 49349-064-02
Proprietary Name CALCIUM ACETATE
Package Description 30 CAPSULE in 1 BLISTER PACK (49349-064-02)
Product NDC 49349-064
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CALCIUM ACETATE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101111
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name CALCIUM ACETATE
Strength Number 667
Strength Unit mg/1
Pharmaceutical Classes Calcium [Chemical/Ingredient],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA]

Complete Information of CALCIUM ACETATE


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