Product NDC: | 54868-5691 |
Proprietary Name: | Phoslo |
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) |
Product NDC: | 54868-5691 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021160 |
Marketing Category: | NDA |
Start Marketing Date: | 20100301 |
Package NDC: | 54868-5691-0 |
Package Description: | 200 CAPSULE in 1 BOTTLE (54868-5691-0) |
NDC Code | 54868-5691-0 |
Proprietary Name | Phoslo |
Package Description | 200 CAPSULE in 1 BOTTLE (54868-5691-0) |
Product NDC | 54868-5691 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Calcium Acetate |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20100301 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, 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] |