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NATALVIRT CA
NATALVIRT CA - 76439-244-60 - (CALCIUM CITRATE, IRON PENTACARBONYL, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, DL-, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, DOCUSATE SODIUM, ASCORBIC ACID, THIAMINE, RIBOFLAVIN, NIACINAMIDE, POTASSIUM IODIDE, ZINC OXIDE, CUPRIC OXIDE, and DOCONEXENT)
Drug Information of NATALVIRT CA
| Product NDC: | 76439-244 |
| Proprietary Name: | NATALVIRT CA |
| Non Proprietary Name: | CALCIUM CITRATE, IRON PENTACARBONYL, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, DL-, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, DOCUSATE SODIUM, ASCORBIC ACID, THIAMINE, RIBOFLAVIN, NIACINAMIDE, POTASSIUM IODIDE, ZINC OXIDE, CUPRIC OXIDE, 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, POTASSIUM IODIDE, ZINC OXIDE, CUPRIC OXIDE, and DOCONEXENT |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NATALVIRT CA
| Product NDC: | 76439-244 |
| Labeler Name: | Virtus Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20130115 |
Package Information of NATALVIRT CA
| Package NDC: | 76439-244-60 |
| Package Description: | 1 KIT in 1 CARTON (76439-244-60) * 30 TABLET in 1 BLISTER PACK * 30 CAPSULE, GELATIN COATED in 1 BLISTER PACK |
NDC Information of NATALVIRT CA
| NDC Code | 76439-244-60 |
| Proprietary Name | NATALVIRT CA |
| Package Description | 1 KIT in 1 CARTON (76439-244-60) * 30 TABLET in 1 BLISTER PACK * 30 CAPSULE, GELATIN COATED in 1 BLISTER PACK |
| Product NDC | 76439-244 |
| 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, POTASSIUM IODIDE, ZINC OXIDE, CUPRIC OXIDE, 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 | |
| Pharmaceutical Classes |
