| 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] |