Product NDC: | 13811-606 |
Proprietary Name: | TL-HEM 150 |
Non Proprietary Name: | Ascorbic Acid, .Alpha.-Tocopherol Acetate, DL-, Folic Acid, Cyanocobalamin, Biotin, Iron, Cupric Sulfate, and Docusate Sodium |
Active Ingredient(s): | 30; 500; 150; 3; 60; 50; 1; 150 [iU]/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; mg/1 & nbsp; Ascorbic Acid, .Alpha.-Tocopherol Acetate, DL-, Folic Acid, Cyanocobalamin, Biotin, Iron, Cupric Sulfate, and Docusate Sodium |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 13811-606 |
Labeler Name: | TRIGEN Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110101 |
Package NDC: | 13811-606-90 |
Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (13811-606-90) |
NDC Code | 13811-606-90 |
Proprietary Name | TL-HEM 150 |
Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (13811-606-90) |
Product NDC | 13811-606 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ascorbic Acid, .Alpha.-Tocopherol Acetate, DL-, Folic Acid, Cyanocobalamin, Biotin, Iron, Cupric Sulfate, and Docusate Sodium |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20110101 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | TRIGEN Laboratories, Inc. |
Substance Name | .ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; BIOTIN; CUPRIC SULFATE; CYANOCOBALAMIN; DOCUSATE SODIUM; FOLIC ACID; IRON |
Strength Number | 30; 500; 150; 3; 60; 50; 1; 150 |
Strength Unit | [iU]/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; mg/1 |
Pharmaceutical Classes | Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC] |