 
                        | Product NDC: | 36987-2004 | 
| Proprietary Name: | Mucor plumbeus | 
| Non Proprietary Name: | Mucor plumbeus | 
| Active Ingredient(s): | 20000 [PNU]/mL & nbsp; Mucor plumbeus | 
| Administration Route(s): | INTRADERMAL; SUBCUTANEOUS | 
| Dosage Form(s): | INJECTION, SOLUTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 36987-2004 | 
| Labeler Name: | Nelco Laboratories, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | BLA102192 | 
| Marketing Category: | BLA | 
| Start Marketing Date: | 19720829 | 
| Package NDC: | 36987-2004-4 | 
| Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (36987-2004-4) | 
| NDC Code | 36987-2004-4 | 
| Proprietary Name | Mucor plumbeus | 
| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (36987-2004-4) | 
| Product NDC | 36987-2004 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Mucor plumbeus | 
| Dosage Form Name | INJECTION, SOLUTION | 
| Route Name | INTRADERMAL; SUBCUTANEOUS | 
| Start Marketing Date | 19720829 | 
| Marketing Category Name | BLA | 
| Labeler Name | Nelco Laboratories, Inc. | 
| Substance Name | MUCOR PLUMBEUS | 
| Strength Number | 20000 | 
| Strength Unit | [PNU]/mL | 
| Pharmaceutical Classes | Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient] |