 
                        | Product NDC: | 49288-0298 | 
| Proprietary Name: | Microsporum audouinii | 
| Non Proprietary Name: | Microsporum audouinii | 
| Active Ingredient(s): | .05 g/mL & nbsp; Microsporum audouinii | 
| Administration Route(s): | INTRADERMAL; SUBCUTANEOUS | 
| Dosage Form(s): | INJECTION, SOLUTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 49288-0298 | 
| Labeler Name: | Antigen Laboratories, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | BLA102223 | 
| Marketing Category: | BLA | 
| Start Marketing Date: | 19740323 | 
| Package NDC: | 49288-0298-5 | 
| Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (49288-0298-5) | 
| NDC Code | 49288-0298-5 | 
| Proprietary Name | Microsporum audouinii | 
| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (49288-0298-5) | 
| Product NDC | 49288-0298 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Microsporum audouinii | 
| Dosage Form Name | INJECTION, SOLUTION | 
| Route Name | INTRADERMAL; SUBCUTANEOUS | 
| Start Marketing Date | 19740323 | 
| Marketing Category Name | BLA | 
| Labeler Name | Antigen Laboratories, Inc. | 
| Substance Name | MICROSPORUM AUDOUINII | 
| Strength Number | .05 | 
| Strength Unit | g/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] |