Product NDC: | 52747-904 |
Proprietary Name: | Tandem DHA |
Non Proprietary Name: | Vitamin- Mineral Omega-3 Supplement |
Active Ingredient(s): | 20; 15; 1; 15; 310.1; 25 mg/1; mg/1; mg/1; mg/1; mg/1; mg/1 & nbsp; Vitamin- Mineral Omega-3 Supplement |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52747-904 |
Labeler Name: | US Pharmaceutical Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20070117 |
Package NDC: | 52747-904-60 |
Package Description: | 90 CAPSULE in 1 BOTTLE, PLASTIC (52747-904-60) |
NDC Code | 52747-904-60 |
Proprietary Name | Tandem DHA |
Package Description | 90 CAPSULE in 1 BOTTLE, PLASTIC (52747-904-60) |
Product NDC | 52747-904 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Vitamin- Mineral Omega-3 Supplement |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20070117 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | US Pharmaceutical Corporation |
Substance Name | ASCORBIC ACID; FERROUS FUMARATE; FOLIC ACID; IRON; OMEGA-3-ACID ETHYL ESTERS; PYRIDOXINE HYDROCHLORIDE |
Strength Number | 20; 15; 1; 15; 310.1; 25 |
Strength Unit | mg/1; mg/1; mg/1; mg/1; mg/1; mg/1 |
Pharmaceutical Classes |