| 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] |