Kentucky Bluegrass (June), Standardized is a Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Alk-abello, Inc.. The primary component is Poa Pratensis Pollen.
| Product ID | 0268-0283_13f1ef62-876b-4a9f-90cd-bb7e307157e9 |
| NDC | 0268-0283 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Kentucky Bluegrass (June), Standardized |
| Generic Name | Kentucky Bluegrass (june), Standardized |
| Dosage Form | Injection, Solution |
| Route of Administration | SUBCUTANEOUS |
| Marketing Start Date | 1997-12-18 |
| Marketing Category | BLA / BLA |
| Application Number | BLA103052 |
| Labeler Name | ALK-Abello, Inc. |
| Substance Name | POA PRATENSIS POLLEN |
| Active Ingredient Strength | 100000 [BAU]/mL |
| Pharm Classes | 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 | 2018-12-31 |
| Marketing Start Date | 1997-12-18 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | BLA |
| Application Number | BLA103052 |
| Product Type | STANDARDIZED ALLERGENIC |
| Marketing Start Date | 1997-12-18 |
| Marketing Category | BLA |
| Application Number | BLA103052 |
| Product Type | STANDARDIZED ALLERGENIC |
| Billing Unit | ML |
| Marketing Start Date | 1997-12-18 |
| Ingredient | Strength |
|---|---|
| POA PRATENSIS POLLEN | 100000 [BAU]/mL |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0268-0283 | Kentucky Bluegrass (June), Standardized | Kentucky Bluegrass (June), Standardized |
| 0268-0284 | Kentucky Bluegrass (June), Standardized | Kentucky Bluegrass (June), Standardized |
| 0268-3051 | Kentucky Bluegrass (June), Standardized | Kentucky Bluegrass (June), Standardized |
| 0268-3052 | Kentucky Bluegrass (June), Standardized | Kentucky Bluegrass (June), Standardized |