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Natelle One
Natelle One - 18860-852-00 - (Natelle One)
Drug Information of Natelle One
| Product NDC: | 18860-852 |
| Proprietary Name: | Natelle One |
| Non Proprietary Name: | Natelle One |
| Active Ingredient(s): | 30; 30; 250; 27; 1; .625; 25; 100 [iU]/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1 & nbsp; Natelle One |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, GELATIN COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Natelle One
| Product NDC: | 18860-852 |
| Labeler Name: | Azur Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | na |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20091109 |
Package Information of Natelle One
| Package NDC: | 18860-852-00 |
| Package Description: | 5 CAPSULE, GELATIN COATED in 1 BLISTER PACK (18860-852-00) |
NDC Information of Natelle One
| NDC Code | 18860-852-00 |
| Proprietary Name | Natelle One |
| Package Description | 5 CAPSULE, GELATIN COATED in 1 BLISTER PACK (18860-852-00) |
| Product NDC | 18860-852 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Natelle One |
| Dosage Form Name | CAPSULE, GELATIN COATED |
| Route Name | ORAL |
| Start Marketing Date | 20091109 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Azur Pharma, Inc. |
| Substance Name | ALPHA-TOCOPHEROL, D-; ASCORBIC ACID; DOCONEXENT; FERROUS FUMARATE; FOLIC ACID; ICOSAPENT; PYRIDOXINE HYDROCHLORIDE; TRICALCIUM PHOSPHATE |
| Strength Number | 30; 30; 250; 27; 1; .625; 25; 100 |
| 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] |
