Product NDC: | 0078-0149 |
Proprietary Name: | Miacalcin |
Non Proprietary Name: | calcitonin salmon |
Active Ingredient(s): | 200 [iU]/mL & nbsp; calcitonin salmon |
Administration Route(s): | INTRAMUSCULAR; SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0078-0149 |
Labeler Name: | Novartis Pharmaceuticals Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017808 |
Marketing Category: | NDA |
Start Marketing Date: | 19860703 |
Package NDC: | 0078-0149-23 |
Package Description: | 2 mL in 1 VIAL (0078-0149-23) |
NDC Code | 0078-0149-23 |
Proprietary Name | Miacalcin |
Package Description | 2 mL in 1 VIAL (0078-0149-23) |
Product NDC | 0078-0149 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | calcitonin salmon |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR; SUBCUTANEOUS |
Start Marketing Date | 19860703 |
Marketing Category Name | NDA |
Labeler Name | Novartis Pharmaceuticals Corporation |
Substance Name | CALCITONIN SALMON |
Strength Number | 200 |
Strength Unit | [iU]/mL |
Pharmaceutical Classes | Calcitonin [Chemical/Ingredient],Calcitonin [EPC] |