Product NDC: | 55154-6809 |
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) |
Product NDC: | 55154-6809 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19960123 |
Package NDC: | 55154-6809-0 |
Package Description: | 10 POUCH in 1 BAG (55154-6809-0) > 1 TABLET in 1 POUCH |
NDC Code | 55154-6809-0 |
Proprietary Name | Calgest |
Package Description | 10 POUCH in 1 BAG (55154-6809-0) > 1 TABLET in 1 POUCH |
Product NDC | 55154-6809 |
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 | Cardinal Health |
Substance Name | CALCIUM CARBONATE |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes |