| NDC Code | 49643-114-10 |
|---|
| Package Description | 10 mL in 1 VIAL, MULTI-DOSE (49643-114-10) |
|---|
| Product NDC | 49643-114 |
|---|
| Product Type Name | NON-STANDARDIZED ALLERGENIC |
|---|
| Proprietary Name | Mucor |
|---|
| Non-Proprietary Name | Mucor Racemosus |
|---|
| Dosage Form | INJECTION |
|---|
| Usage | CUTANEOUS; INTRADERMAL; SUBCUTANEOUS |
|---|
| Start Marketing Date | 19740312 |
|---|
| Marketing Category Name | BLA |
|---|
| Application Number | BLA102211 |
|---|
| Manufacturer | Allermed Laboratories, Inc. |
|---|
| Substance Name | MUCOR RACEMOSUS |
|---|
| Strength | .1 |
|---|
| Strength Unit | g/mL |
|---|
| Pharmacy Classes | Allergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC] |
|---|