Product NDC: | 51861-102 |
Proprietary Name: | PRENATAL CHELATED MINERAL |
Non Proprietary Name: | CALCIUM CITRATE, CALCIUM CARBONATE, POTASSIUM IODIDE, MAGNESIUM CITRATE, ZINC CITRATE, COPPER GLUCONATE, and FERROUS FUMARATE |
Active Ingredient(s): | 30; 32.5; .5; 7; 75; 75; 5 mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1 & nbsp; CALCIUM CITRATE, CALCIUM CARBONATE, POTASSIUM IODIDE, MAGNESIUM CITRATE, ZINC CITRATE, COPPER GLUCONATE, and FERROUS FUMARATE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51861-102 |
Labeler Name: | USANA Health Sciences, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20120411 |
Package NDC: | 51861-102-88 |
Package Description: | 112 TABLET in 1 BOTTLE (51861-102-88) |
NDC Code | 51861-102-88 |
Proprietary Name | PRENATAL CHELATED MINERAL |
Package Description | 112 TABLET in 1 BOTTLE (51861-102-88) |
Product NDC | 51861-102 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | CALCIUM CITRATE, CALCIUM CARBONATE, POTASSIUM IODIDE, MAGNESIUM CITRATE, ZINC CITRATE, COPPER GLUCONATE, and FERROUS FUMARATE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120411 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | USANA Health Sciences, Inc. |
Substance Name | CALCIUM CARBONATE; CALCIUM CITRATE; COPPER GLUCONATE; FERROUS FUMARATE; MAGNESIUM CITRATE; POTASSIUM IODIDE; ZINC CITRATE |
Strength Number | 30; 32.5; .5; 7; 75; 75; 5 |
Strength Unit | mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1 |
Pharmaceutical Classes |