Mixture of Standardized Mites is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Antigen Laboratories, Inc.. The primary component is Dermatophagoides Pteronyssinus; Dermatophagoides Farinae.
| Product ID | 49288-0182_745162a9-2fdc-4b03-a3bc-32d410b3d9c1 |
| NDC | 49288-0182 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Mixture of Standardized Mites |
| Generic Name | Mixture Of Standardized Mites |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRADERMAL; SUBCUTANEOUS |
| Marketing Start Date | 1991-10-22 |
| Marketing Category | BLA / BLA |
| Application Number | BLA102225 |
| Labeler Name | Antigen Laboratories, Inc. |
| Substance Name | DERMATOPHAGOIDES PTERONYSSINUS; DERMATOPHAGOIDES FARINAE |
| Active Ingredient Strength | 5000 [AU]/mL; [AU]/mL |
| Pharm Classes | Standardized Insect Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Antigens, Dermatophagoides [CS],Insect Proteins [CS],Allergens [CS],Allergens [CS],Insect Proteins [CS],Standardized Insect Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Antigens, Dermatophagoides [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 1991-10-22 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | BLA |
| Application Number | BLA102225 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1991-10-22 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | BLA |
| Application Number | BLA102225 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1991-10-22 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | BLA |
| Application Number | BLA102225 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1991-10-22 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | BLA |
| Application Number | BLA102225 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1991-10-22 |
| Inactivation Date | 2019-10-21 |
| Ingredient | Strength |
|---|---|
| DERMATOPHAGOIDES PTERONYSSINUS | 5000 [AU]/mL |
| SPL SET ID: | 3b3cb12c-65d3-46ab-9bac-82c569a76220 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |