Product NDC: | 0517-0031 |
Proprietary Name: | Cyanocobalamin |
Non Proprietary Name: | cyanocobalamin |
Active Ingredient(s): | 1000 ug/mL & nbsp; cyanocobalamin |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0517-0031 |
Labeler Name: | American Regent, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA080737 |
Marketing Category: | ANDA |
Start Marketing Date: | 19900930 |
Package NDC: | 0517-0031-25 |
Package Description: | 25 VIAL, SINGLE-USE in 1 TRAY (0517-0031-25) > 1 mL in 1 VIAL, SINGLE-USE |
NDC Code | 0517-0031-25 |
Proprietary Name | Cyanocobalamin |
Package Description | 25 VIAL, SINGLE-USE in 1 TRAY (0517-0031-25) > 1 mL in 1 VIAL, SINGLE-USE |
Product NDC | 0517-0031 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | cyanocobalamin |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 19900930 |
Marketing Category Name | ANDA |
Labeler Name | American Regent, Inc. |
Substance Name | CYANOCOBALAMIN |
Strength Number | 1000 |
Strength Unit | ug/mL |
Pharmaceutical Classes | Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC] |