Product NDC: | 0904-5513 |
Proprietary Name: | antacid |
Non Proprietary Name: | Calcium carbonate |
Active Ingredient(s): | 750 mg/1 & nbsp; Calcium carbonate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, CHEWABLE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0904-5513 |
Labeler Name: | Major Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20010320 |
Package NDC: | 0904-5513-79 |
Package Description: | 96 TABLET, CHEWABLE in 1 BOTTLE (0904-5513-79) |
NDC Code | 0904-5513-79 |
Proprietary Name | antacid |
Package Description | 96 TABLET, CHEWABLE in 1 BOTTLE (0904-5513-79) |
Product NDC | 0904-5513 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Calcium carbonate |
Dosage Form Name | TABLET, CHEWABLE |
Route Name | ORAL |
Start Marketing Date | 20010320 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Major Pharmaceuticals |
Substance Name | CALCIUM CARBONATE |
Strength Number | 750 |
Strength Unit | mg/1 |
Pharmaceutical Classes |