| Product NDC: | 0781-6320 |
| Proprietary Name: | calcitonin salmon |
| Non Proprietary Name: | calcitonin salmon |
| Active Ingredient(s): | 200 [iU]/1 & nbsp; calcitonin salmon |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0781-6320 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020313 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19950801 |
| Package NDC: | 0781-6320-79 |
| Package Description: | 1 BOTTLE, GLASS in 1 BOX (0781-6320-79) > 30 SPRAY, METERED in 1 BOTTLE, GLASS |
| NDC Code | 0781-6320-79 |
| Proprietary Name | calcitonin salmon |
| Package Description | 1 BOTTLE, GLASS in 1 BOX (0781-6320-79) > 30 SPRAY, METERED in 1 BOTTLE, GLASS |
| Product NDC | 0781-6320 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | calcitonin salmon |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 19950801 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Sandoz Inc |
| Substance Name | CALCITONIN SALMON |
| Strength Number | 200 |
| Strength Unit | [iU]/1 |
| Pharmaceutical Classes | Calcitonin [Chemical/Ingredient],Calcitonin [EPC] |