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Calcium carbonate
Calcium carbonate - 0536-3414-10 - (Calcium carbonate)
Drug Information of Calcium carbonate
| Product NDC: | 0536-3414 |
| 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: | 0536-3414 |
| Labeler Name: | Rugby Laboratories Inc. |
| 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: | 0536-3414-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE (0536-3414-10) |
NDC Information of Calcium carbonate
| NDC Code | 0536-3414-10 |
| Proprietary Name | Calcium carbonate |
| Package Description | 1000 TABLET in 1 BOTTLE (0536-3414-10) |
| Product NDC | 0536-3414 |
| 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 | Rugby Laboratories Inc. |
| Substance Name | CALCIUM CARBONATE |
| Strength Number | 648 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
