| Product NDC: | 35418-310 |
| Proprietary Name: | Trial Antacid |
| Non Proprietary Name: | Calcium Carbonate |
| Active Ingredient(s): | 420 mg/1 & nbsp; Calcium Carbonate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 35418-310 |
| Labeler Name: | Zee Medical Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120612 |
| Package NDC: | 35418-310-69 |
| Package Description: | 500 CARTON in 1 CARTON (35418-310-69) > 50 CARTON in 1 CARTON (35418-310-68) > 125 PACKET in 1 CARTON (35418-310-67) > 2 TABLET in 1 PACKET (35418-310-02) |
| NDC Code | 35418-310-69 |
| Proprietary Name | Trial Antacid |
| Package Description | 500 CARTON in 1 CARTON (35418-310-69) > 50 CARTON in 1 CARTON (35418-310-68) > 125 PACKET in 1 CARTON (35418-310-67) > 2 TABLET in 1 PACKET (35418-310-02) |
| Product NDC | 35418-310 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Calcium Carbonate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120612 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Zee Medical Inc |
| Substance Name | CALCIUM CARBONATE |
| Strength Number | 420 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |