Home
>
National Drug Code (NDC)
>
antacid
antacid - 41250-489-82 - (Calcium carbonate)
Drug Information of antacid
| Product NDC: | 41250-489 |
| 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) |
Labeler Information of antacid
| Product NDC: | 41250-489 |
| Labeler Name: | Meijer Distribution Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20000720 |
Package Information of antacid
| Package NDC: | 41250-489-82 |
| Package Description: | 200 TABLET, CHEWABLE in 1 BOTTLE (41250-489-82) |
NDC Information of antacid
| NDC Code | 41250-489-82 |
| Proprietary Name | antacid |
| Package Description | 200 TABLET, CHEWABLE in 1 BOTTLE (41250-489-82) |
| Product NDC | 41250-489 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Calcium carbonate |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20000720 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Meijer Distribution Inc |
| Substance Name | CALCIUM CARBONATE |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
