Product NDC: | 49884-161 |
Proprietary Name: | CALCITONIN SALMON |
Non Proprietary Name: | CALCITONIN SALMON |
Active Ingredient(s): | 200 [iU]/.09mL & nbsp; CALCITONIN SALMON |
Administration Route(s): | NASAL |
Dosage Form(s): | SPRAY, METERED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49884-161 |
Labeler Name: | Par Pharmaceutical Inc. (mgc) |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076979 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090608 |
Package NDC: | 49884-161-11 |
Package Description: | 3.8 mL in 1 BOTTLE, GLASS (49884-161-11) |
NDC Code | 49884-161-11 |
Proprietary Name | CALCITONIN SALMON |
Package Description | 3.8 mL in 1 BOTTLE, GLASS (49884-161-11) |
Product NDC | 49884-161 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CALCITONIN SALMON |
Dosage Form Name | SPRAY, METERED |
Route Name | NASAL |
Start Marketing Date | 20090608 |
Marketing Category Name | ANDA |
Labeler Name | Par Pharmaceutical Inc. (mgc) |
Substance Name | CALCITONIN SALMON |
Strength Number | 200 |
Strength Unit | [iU]/.09mL |
Pharmaceutical Classes | Calcitonin [Chemical/Ingredient],Calcitonin [EPC] |