Standardized Redtop Grass is a Cutaneous; Intradermal; Subcutaneous Injection in the Human Prescription Drug category. It is labeled and distributed by Allermed Laboratories, Inc.. The primary component is Agrostis Gigantea Pollen.
Product ID | 49643-309_92edfda3-37dd-daa1-e053-2a95a90a5c1f |
NDC | 49643-309 |
Product Type | Human Prescription Drug |
Proprietary Name | Standardized Redtop Grass |
Generic Name | Agrostis Alba |
Dosage Form | Injection |
Route of Administration | CUTANEOUS; INTRADERMAL; SUBCUTANEOUS |
Marketing Start Date | 1996-12-02 |
Marketing Category | BLA / BLA |
Application Number | BLA102218 |
Labeler Name | Allermed Laboratories, Inc. |
Substance Name | AGROSTIS GIGANTEA POLLEN |
Active Ingredient Strength | 100000 [BAU]/mL |
Pharm Classes | Standardized Pollen Allergenic Extract [EPC],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 1996-12-02 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | BLA |
Application Number | BLA102218 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1996-12-02 |
Marketing Category | BLA |
Application Number | BLA102218 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1996-12-02 |
Marketing Category | BLA |
Application Number | BLA102218 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1996-12-02 |
Marketing Category | BLA |
Application Number | BLA102218 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1996-12-02 |
Ingredient | Strength |
---|---|
AGROSTIS GIGANTEA POLLEN | 100000 [BAU]/mL |
NDC | Brand Name | Generic Name |
---|---|---|
49643-309 | Standardized Redtop Grass | Agrostis alba |
22840-0207 | Standardized Redtop Pollen | Agrostis alba |
22840-0208 | Standardized Redtop Pollen | Agrostis alba |