Product NDC: | 18860-752 |
Proprietary Name: | Natelle One |
Non Proprietary Name: | doconexent,icosapent, tricalcium phosphate, ferrous fumarate, ascorbic acid, pyridoxine hydrochloride, alpha-tocopherol, and folic acid |
Active Ingredient(s): | 30; 30; 250; 28; 1; .625; 25; 102 [iU]/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1 & nbsp; doconexent,icosapent, tricalcium phosphate, ferrous fumarate, ascorbic acid, pyridoxine hydrochloride, alpha-tocopherol, and folic acid |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, GELATIN COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 18860-752 |
Labeler Name: | Jazz Pharmaceuticals Commercial Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100611 |
Package NDC: | 18860-752-00 |
Package Description: | 3 CAPSULE, GELATIN COATED in 1 BLISTER PACK (18860-752-00) |
NDC Code | 18860-752-00 |
Proprietary Name | Natelle One |
Package Description | 3 CAPSULE, GELATIN COATED in 1 BLISTER PACK (18860-752-00) |
Product NDC | 18860-752 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | doconexent,icosapent, tricalcium phosphate, ferrous fumarate, ascorbic acid, pyridoxine hydrochloride, alpha-tocopherol, and folic acid |
Dosage Form Name | CAPSULE, GELATIN COATED |
Route Name | ORAL |
Start Marketing Date | 20100611 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Jazz Pharmaceuticals Commercial Corp. |
Substance Name | .ALPHA.-TOCOPHEROL; ASCORBIC ACID; DOCONEXENT; FERROUS FUMARATE; FOLIC ACID; ICOSAPENT; PYRIDOXINE HYDROCHLORIDE; TRICALCIUM PHOSPHATE |
Strength Number | 30; 30; 250; 28; 1; .625; 25; 102 |
Strength Unit | [iU]/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1 |
Pharmaceutical Classes | Calcium [Chemical/Ingredient],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA] |