Product NDC: | 76439-245 |
Proprietary Name: | NATALVIRT 90DHA |
Non Proprietary Name: | CALCIUM CITRATE, IRON PENTACARBONYL, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, DL-, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, DOCUSATE SODIUM, ASCORBIC ACID, THIAMINE, RIBOFLAVIN, NIACINAMIDE, IODINE, ZINC, COPPER, and DOCONEXENT |
Active Ingredient(s): | & nbsp; CALCIUM CITRATE, IRON PENTACARBONYL, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, DL-, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, DOCUSATE SODIUM, ASCORBIC ACID, THIAMINE, RIBOFLAVIN, NIACINAMIDE, IODINE, ZINC, COPPER, and DOCONEXENT |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76439-245 |
Labeler Name: | Virtus Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20130115 |
Package NDC: | 76439-245-60 |
Package Description: | 1 KIT in 1 CARTON (76439-245-60) * 30 TABLET in 1 BLISTER PACK * 30 CAPSULE, GELATIN COATED in 1 BLISTER PACK |
NDC Code | 76439-245-60 |
Proprietary Name | NATALVIRT 90DHA |
Package Description | 1 KIT in 1 CARTON (76439-245-60) * 30 TABLET in 1 BLISTER PACK * 30 CAPSULE, GELATIN COATED in 1 BLISTER PACK |
Product NDC | 76439-245 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CALCIUM CITRATE, IRON PENTACARBONYL, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, DL-, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, DOCUSATE SODIUM, ASCORBIC ACID, THIAMINE, RIBOFLAVIN, NIACINAMIDE, IODINE, ZINC, COPPER, and DOCONEXENT |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20130115 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Virtus Pharmaceuticals |
Substance Name | |
Strength Number | |
Strength Unit | |
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