Home
>
National Drug Code (NDC)
>
Calgest
Calgest - 0536-4742-97 - (Calgest)
Drug Information of Calgest
| Product NDC: | 0536-4742 |
| Proprietary Name: | Calgest |
| Non Proprietary Name: | Calgest |
| Active Ingredient(s): | 500 mg/1 & nbsp; Calgest |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Calgest
| Product NDC: | 0536-4742 |
| Labeler Name: | Rugby Laboratories Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19960123 |
Package Information of Calgest
| Package NDC: | 0536-4742-97 |
| Package Description: | 150 TABLET in 1 BOTTLE (0536-4742-97) |
NDC Information of Calgest
| NDC Code | 0536-4742-97 |
| Proprietary Name | Calgest |
| Package Description | 150 TABLET in 1 BOTTLE (0536-4742-97) |
| Product NDC | 0536-4742 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Calgest |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19960123 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rugby Laboratories Inc. |
| Substance Name | CALCIUM CARBONATE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
