| NDC Code: |
18860-852 |
| Proprietary Name: |
Natelle One |
| Suffix: |
|
| Non-Proprietary Name: |
Natelle One |
| Dosage Form: |
CAPSULE, GELATIN COATED |
| Method: |
ORAL |
| Original Marketing Date: |
09-11-2009 |
| Category Name: |
UNAPPROVED DRUG OTHER |
| Application Number: |
na |
| Labeler: |
AZUR PHARMA, INC. |
| Substance Name: |
ALPHA-TOCOPHEROL, D-; ASCORBIC ACID; DOCONEXENT; FERROUS FUMARATE; FOLIC ACID; ICOSAPENT; PYRIDOXINE HYDROCHLORIDE; TRICALCIUM PHOSPHATE |
| Active Numerator Strength: |
30; 30; 250; 27; 1; .625; 25; 100 |
| Active Ingredient Unit: |
[iU]/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1 |
| Pharm Classes: |
Calcium [Chemical/Ingredient],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA] |
| DEA Schedule: |
|
