Product NDC: | 63323-044 |
Proprietary Name: | Cyanocobalamin |
Non Proprietary Name: | CYANOCOBALAMIN |
Active Ingredient(s): | 1000 ug/mL & nbsp; CYANOCOBALAMIN |
Administration Route(s): | INTRAMUSCULAR; SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63323-044 |
Labeler Name: | APP Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA080557 |
Marketing Category: | ANDA |
Start Marketing Date: | 20001018 |
Package NDC: | 63323-044-01 |
Package Description: | 25 VIAL, MULTI-DOSE in 1 TRAY (63323-044-01) > 1 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 63323-044-01 |
Proprietary Name | Cyanocobalamin |
Package Description | 25 VIAL, MULTI-DOSE in 1 TRAY (63323-044-01) > 1 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 63323-044 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CYANOCOBALAMIN |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR; SUBCUTANEOUS |
Start Marketing Date | 20001018 |
Marketing Category Name | ANDA |
Labeler Name | APP Pharmaceuticals, LLC |
Substance Name | CYANOCOBALAMIN |
Strength Number | 1000 |
Strength Unit | ug/mL |
Pharmaceutical Classes | Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC] |