 
                        | Product NDC: | 49884-270 | 
| Proprietary Name: | Nascobal | 
| Non Proprietary Name: | cyanocobalamin | 
| Active Ingredient(s): | 500 ug/1 & nbsp; cyanocobalamin | 
| Administration Route(s): | NASAL | 
| Dosage Form(s): | SPRAY | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 49884-270 | 
| Labeler Name: | Par Pharmaceutical , Inc | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | NDA021642 | 
| Marketing Category: | NDA | 
| Start Marketing Date: | 20090813 | 
| Package NDC: | 49884-270-86 | 
| Package Description: | 4 SPRAY in 1 BOTTLE (49884-270-86) | 
| NDC Code | 49884-270-86 | 
| Proprietary Name | Nascobal | 
| Package Description | 4 SPRAY in 1 BOTTLE (49884-270-86) | 
| Product NDC | 49884-270 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | cyanocobalamin | 
| Dosage Form Name | SPRAY | 
| Route Name | NASAL | 
| Start Marketing Date | 20090813 | 
| Marketing Category Name | NDA | 
| Labeler Name | Par Pharmaceutical , Inc | 
| Substance Name | CYANOCOBALAMIN | 
| Strength Number | 500 | 
| Strength Unit | ug/1 | 
| Pharmaceutical Classes | Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC] |