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Natelle One - 18860-852-00 - (Natelle One)

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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]

Complete Information of Natelle One


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