Product NDC: | 63736-176 |
Proprietary Name: | Chooz |
Non Proprietary Name: | Calcium Carbonate |
Active Ingredient(s): | 500 mg/1 & nbsp; Calcium Carbonate |
Administration Route(s): | ORAL |
Dosage Form(s): | GUM, CHEWING |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63736-176 |
Labeler Name: | Insight Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090610 |
Package NDC: | 63736-176-12 |
Package Description: | 12 GUM, CHEWING in 1 BOX (63736-176-12) |
NDC Code | 63736-176-12 |
Proprietary Name | Chooz |
Package Description | 12 GUM, CHEWING in 1 BOX (63736-176-12) |
Product NDC | 63736-176 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Calcium Carbonate |
Dosage Form Name | GUM, CHEWING |
Route Name | ORAL |
Start Marketing Date | 20090610 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Insight Pharmaceuticals |
Substance Name | CALCIUM CARBONATE |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes |