Product NDC: | 50332-0106 |
Proprietary Name: | NUTRALOX |
Non Proprietary Name: | CALCIUM CARBONATE |
Active Ingredient(s): | 420 mg/1 & nbsp; CALCIUM CARBONATE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, CHEWABLE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50332-0106 |
Labeler Name: | HART Health |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19870120 |
Package NDC: | 50332-0106-3 |
Package Description: | 20 PACKET in 1 BOX, UNIT-DOSE (50332-0106-3) > 2 TABLET, CHEWABLE in 1 PACKET |
NDC Code | 50332-0106-3 |
Proprietary Name | NUTRALOX |
Package Description | 20 PACKET in 1 BOX, UNIT-DOSE (50332-0106-3) > 2 TABLET, CHEWABLE in 1 PACKET |
Product NDC | 50332-0106 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | CALCIUM CARBONATE |
Dosage Form Name | TABLET, CHEWABLE |
Route Name | ORAL |
Start Marketing Date | 19870120 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | HART Health |
Substance Name | CALCIUM CARBONATE |
Strength Number | 420 |
Strength Unit | mg/1 |
Pharmaceutical Classes |