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PNV-OB-DHA
PNV-OB-DHA - 42192-352-60 - (.beta.-carotene, cholecalciferol, ascorbic acid, .alpha.-tocopherol acetate, dl-, folic acid, thiamine mononitrate, riboflavin, pyridoxine hydrochloride, cyanocobalamin, niacinamide, calcium carbonate, ferrous fumarate, magnesium oxide, zinc oxide, cupric oxide and doconexent)
Drug Information of PNV-OB-DHA
| Product NDC: | 42192-352 |
| Proprietary Name: | PNV-OB-DHA |
| Non Proprietary Name: | .beta.-carotene, cholecalciferol, ascorbic acid, .alpha.-tocopherol acetate, dl-, folic acid, thiamine mononitrate, riboflavin, pyridoxine hydrochloride, cyanocobalamin, niacinamide, calcium carbonate, ferrous fumarate, magnesium oxide, zinc oxide, cupric oxide and doconexent |
| Active Ingredient(s): | & nbsp; .beta.-carotene, cholecalciferol, ascorbic acid, .alpha.-tocopherol acetate, dl-, folic acid, thiamine mononitrate, riboflavin, pyridoxine hydrochloride, cyanocobalamin, niacinamide, calcium carbonate, ferrous fumarate, magnesium oxide, zinc oxide, cupric oxide and doconexent |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PNV-OB-DHA
| Product NDC: | 42192-352 |
| Labeler Name: | Acella Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20130517 |
Package Information of PNV-OB-DHA
| Package NDC: | 42192-352-60 |
| Package Description: | 30 BLISTER PACK in 1 CARTON (42192-352-60) > 1 KIT in 1 BLISTER PACK |
NDC Information of PNV-OB-DHA
| NDC Code | 42192-352-60 |
| Proprietary Name | PNV-OB-DHA |
| Package Description | 30 BLISTER PACK in 1 CARTON (42192-352-60) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 42192-352 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | .beta.-carotene, cholecalciferol, ascorbic acid, .alpha.-tocopherol acetate, dl-, folic acid, thiamine mononitrate, riboflavin, pyridoxine hydrochloride, cyanocobalamin, niacinamide, calcium carbonate, ferrous fumarate, magnesium oxide, zinc oxide, cupric oxide and doconexent |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20130517 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Acella Pharmaceuticals, LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
