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Calcium carbonate
Calcium carbonate - 63629-3757-1 - (Calcium carbonate)
Drug Information of Calcium carbonate
| Product NDC: | 63629-3757 |
| Proprietary Name: | Calcium carbonate |
| Non Proprietary Name: | Calcium carbonate |
| Active Ingredient(s): | 648 mg/1 & nbsp; Calcium carbonate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Calcium carbonate
| Product NDC: | 63629-3757 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19990412 |
Package Information of Calcium carbonate
| Package NDC: | 63629-3757-1 |
| Package Description: | 60 TABLET in 1 BOTTLE (63629-3757-1) |
NDC Information of Calcium carbonate
| NDC Code | 63629-3757-1 |
| Proprietary Name | Calcium carbonate |
| Package Description | 60 TABLET in 1 BOTTLE (63629-3757-1) |
| Product NDC | 63629-3757 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Calcium carbonate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19990412 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | CALCIUM CARBONATE |
| Strength Number | 648 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
