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] |