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Sunmark Calcium Antacid
Sunmark Calcium Antacid - 49348-195-16 - (Calcium Carbonate)
Drug Information of Sunmark Calcium Antacid
| Product NDC: | 49348-195 |
| Proprietary Name: | Sunmark Calcium Antacid |
| Non Proprietary Name: | Calcium Carbonate |
| Active Ingredient(s): | 1000 mg/1 & nbsp; Calcium Carbonate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunmark Calcium Antacid
| Product NDC: | 49348-195 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20030715 |
Package Information of Sunmark Calcium Antacid
| Package NDC: | 49348-195-16 |
| Package Description: | 72 TABLET, CHEWABLE in 1 BOTTLE (49348-195-16) |
NDC Information of Sunmark Calcium Antacid
| NDC Code | 49348-195-16 |
| Proprietary Name | Sunmark Calcium Antacid |
| Package Description | 72 TABLET, CHEWABLE in 1 BOTTLE (49348-195-16) |
| Product NDC | 49348-195 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Calcium Carbonate |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20030715 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson |
| Substance Name | CALCIUM CARBONATE |
| Strength Number | 1000 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
