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Calcium Acetate
Calcium Acetate - 76237-280-30 - (Calcium Acetate)
Drug Information of Calcium Acetate
| Product NDC: | 76237-280 |
| 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: | 76237-280 |
| Labeler Name: | McKesson Contract Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077728 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130409 |
Package Information of Calcium Acetate
| Package NDC: | 76237-280-30 |
| Package Description: | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-280-30) > 5 CAPSULE in 1 BLISTER PACK |
NDC Information of Calcium Acetate
| NDC Code | 76237-280-30 |
| Proprietary Name | Calcium Acetate |
| Package Description | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-280-30) > 5 CAPSULE in 1 BLISTER PACK |
| Product NDC | 76237-280 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Calcium Acetate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130409 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Contract Packaging |
| 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] |
