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Calcium Carbonate
Calcium Carbonate - 0054-8120-25 - (Calcium Carbonate)
Drug Information of Calcium Carbonate
| Product NDC: | 0054-8120 |
| Proprietary Name: | Calcium Carbonate |
| Non Proprietary Name: | Calcium Carbonate |
| Active Ingredient(s): | 1250 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: | 0054-8120 |
| Labeler Name: | Roxane Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20041118 |
Package Information of Calcium Carbonate
| Package NDC: | 0054-8120-25 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (0054-8120-25) > 10 TABLET in 1 BLISTER PACK |
NDC Information of Calcium Carbonate
| NDC Code | 0054-8120-25 |
| Proprietary Name | Calcium Carbonate |
| Package Description | 10 BLISTER PACK in 1 CARTON (0054-8120-25) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 0054-8120 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Calcium Carbonate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20041118 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Roxane Laboratories, Inc. |
| Substance Name | CALCIUM CARBONATE |
| Strength Number | 1250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
