Rhizopus Mix is a Intradermal; Percutaneous; Subcutaneous Solution in the Non-standardized Allergenic category. It is labeled and distributed by Greer Laboratories, Inc.. The primary component is Rhizopus Stolonifer; Rhizopus Arrhizus.
| Product ID | 22840-9680_77436178-2957-6a77-e053-2a91aa0a873e |
| NDC | 22840-9680 |
| Product Type | Non-standardized Allergenic |
| Proprietary Name | Rhizopus Mix |
| Generic Name | Rhizopus Stolonifer And Rhizopus Oryzae |
| Dosage Form | Solution |
| Route of Administration | INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS |
| Marketing Start Date | 1981-09-15 |
| Marketing Category | BLA / BLA |
| Application Number | BLA101833 |
| Labeler Name | Greer Laboratories, Inc. |
| Substance Name | RHIZOPUS STOLONIFER; RHIZOPUS ARRHIZUS |
| Active Ingredient Strength | 10000 [PNU]/mL; [PNU]/mL |
| Pharm Classes | Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS],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] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 1981-09-15 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | BLA |
| Application Number | BLA101833 |
| Product Type | NON-STANDARDIZED ALLERGENIC |
| Marketing Start Date | 1981-09-15 |
| Ingredient | Strength |
|---|---|
| RHIZOPUS STOLONIFER | 10000 [PNU]/mL |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 22840-9665 | Rhizopus Mix | Rhizopus stolonifer and Rhizopus oryzae |
| 22840-9666 | Rhizopus Mix | Rhizopus stolonifer and Rhizopus oryzae |
| 22840-9668 | Rhizopus Mix | Rhizopus stolonifer and Rhizopus oryzae |
| 22840-9669 | Rhizopus Mix | Rhizopus stolonifer and Rhizopus oryzae |
| 22840-9680 | Rhizopus Mix | Rhizopus stolonifer and Rhizopus oryzae |