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Equaline antacid
Equaline antacid - 41163-595-23 - (Calcium Carbonate)
Drug Information of Equaline antacid
| Product NDC: | 41163-595 |
| Proprietary Name: | Equaline 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 Equaline antacid
| Product NDC: | 41163-595 |
| Labeler Name: | Supervalu Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20041022 |
Package Information of Equaline antacid
| Package NDC: | 41163-595-23 |
| Package Description: | 72 TABLET, CHEWABLE in 1 BOTTLE (41163-595-23) |
NDC Information of Equaline antacid
| NDC Code | 41163-595-23 |
| Proprietary Name | Equaline antacid |
| Package Description | 72 TABLET, CHEWABLE in 1 BOTTLE (41163-595-23) |
| Product NDC | 41163-595 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Calcium Carbonate |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20041022 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Supervalu Inc |
| Substance Name | CALCIUM CARBONATE |
| Strength Number | 1000 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
