| 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] |