 
                        | Product NDC: | 0268-6734 | 
| Proprietary Name: | MORUS RUBRA POLLEN | 
| Non Proprietary Name: | Red Mulberry | 
| Active Ingredient(s): | 1000 [PNU]/mL & nbsp; Red Mulberry | 
| Administration Route(s): | INTRADERMAL | 
| Dosage Form(s): | INJECTION, SOLUTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 0268-6734 | 
| Labeler Name: | ALK-Abello, Inc. | 
| Product Type: | NON-STANDARDIZED ALLERGENIC | 
| FDA Application Number: | BLA103753 | 
| Marketing Category: | BLA | 
| Start Marketing Date: | 19650101 | 
| Package NDC: | 0268-6734-05 | 
| Package Description: | 5 mL in 1 VIAL, MULTI-DOSE (0268-6734-05) | 
| NDC Code | 0268-6734-05 | 
| Proprietary Name | MORUS RUBRA POLLEN | 
| Package Description | 5 mL in 1 VIAL, MULTI-DOSE (0268-6734-05) | 
| Product NDC | 0268-6734 | 
| Product Type Name | NON-STANDARDIZED ALLERGENIC | 
| Non Proprietary Name | Red Mulberry | 
| Dosage Form Name | INJECTION, SOLUTION | 
| Route Name | INTRADERMAL | 
| Start Marketing Date | 19650101 | 
| Marketing Category Name | BLA | 
| Labeler Name | ALK-Abello, Inc. | 
| Substance Name | MORUS RUBRA POLLEN | 
| Strength Number | 1000 | 
| Strength Unit | [PNU]/mL | 
| Pharmaceutical Classes | Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient] |