Product NDC: | 30142-076 |
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 |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 30142-076 |
Labeler Name: | The Kroger Co. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101018 |
Package NDC: | 30142-076-25 |
Package Description: | 96 TABLET in 1 BOTTLE (30142-076-25) |
NDC Code | 30142-076-25 |
Proprietary Name | Antacid |
Package Description | 96 TABLET in 1 BOTTLE (30142-076-25) |
Product NDC | 30142-076 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | calcium carbonate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20101018 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | The Kroger Co. |
Substance Name | CALCIUM CARBONATE |
Strength Number | 750 |
Strength Unit | mg/1 |
Pharmaceutical Classes |