Mixture of Standardized and Non-Standardized Inland Grasses 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 Poa Pratensis Pollen; Dactylis Glomerata Pollen; Lolium Perenne Pollen; Agrostis Gigantea Pollen; Phleum Pratense Pollen; Poa Compressa Pollen; Bromus Inermis Pollen.
Product ID | 49288-0241_bb0c98b2-aaa8-49c4-887a-928e3937769c |
NDC | 49288-0241 |
Product Type | Human Prescription Drug |
Proprietary Name | Mixture of Standardized and Non-Standardized Inland Grasses |
Generic Name | Mixture Of Standardized And Non-standardized Inland Grasses |
Dosage Form | Injection, Solution |
Route of Administration | INTRADERMAL; SUBCUTANEOUS |
Marketing Start Date | 1997-06-13 |
Marketing Category | BLA / BLA |
Application Number | BLA103421 |
Labeler Name | Antigen Laboratories, Inc. |
Substance Name | POA PRATENSIS POLLEN; DACTYLIS GLOMERATA POLLEN; LOLIUM PERENNE POLLEN; AGROSTIS GIGANTEA POLLEN; PHLEUM PRATENSE POLLEN; POA COMPRESSA POLLEN; BROMUS INERMIS POLLEN |
Active Ingredient Strength | 14286 [BAU]/mL; [BAU]/mL; [BAU]/mL; [BAU]/mL; [BAU]/mL; g/mL; g/mL |
Pharm Classes | Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],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],Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],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 | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 1997-06-13 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | BLA |
Application Number | BLA103421 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-06-13 |
Inactivation Date | 2019-10-21 |
Marketing Category | BLA |
Application Number | BLA103421 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-06-13 |
Inactivation Date | 2019-10-21 |
Marketing Category | BLA |
Application Number | BLA103421 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-06-13 |
Inactivation Date | 2019-10-21 |
Ingredient | Strength |
---|---|
POA PRATENSIS POLLEN | 14286 [BAU]/mL |
SPL SET ID: | c08f73ff-4f15-449c-9507-c422367f106b |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |