Product NDC: | 63044-635 |
Proprietary Name: | TRICON |
Non Proprietary Name: | TRICON |
Active Ingredient(s): | 75; 15; 110; .5 mg/1; ug/1; mg/1; mg/1 & nbsp; TRICON |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63044-635 |
Labeler Name: | Nnodum Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20050520 |
Package NDC: | 63044-635-10 |
Package Description: | 10 BLISTER PACK in 1 BOX (63044-635-10) > 10 CAPSULE in 1 BLISTER PACK |
NDC Code | 63044-635-10 |
Proprietary Name | TRICON |
Package Description | 10 BLISTER PACK in 1 BOX (63044-635-10) > 10 CAPSULE in 1 BLISTER PACK |
Product NDC | 63044-635 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | TRICON |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20050520 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Nnodum Pharmaceuticals |
Substance Name | ASCORBIC ACID; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID |
Strength Number | 75; 15; 110; .5 |
Strength Unit | mg/1; ug/1; mg/1; mg/1 |
Pharmaceutical Classes | Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC] |