Hackberry Pollen 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 Celtis Occidentalis Pollen.
| Product ID | 22840-2409_83d281e9-375b-7e6c-e053-2991aa0a6f0e |
| NDC | 22840-2409 |
| Product Type | Non-standardized Allergenic |
| Proprietary Name | Hackberry Pollen |
| Generic Name | Celtis Occidentalis |
| 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 | CELTIS OCCIDENTALIS POLLEN |
| Active Ingredient Strength | 40000 [PNU]/mL |
| Pharm Classes | 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 | 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 |
| Marketing Category | BLA |
| Application Number | BLA101833 |
| Product Type | NON-STANDARDIZED ALLERGENIC |
| Marketing Start Date | 1981-09-15 |
| Ingredient | Strength |
|---|---|
| CELTIS OCCIDENTALIS POLLEN | 40000 [PNU]/mL |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 22840-2408 | Hackberry Pollen | Celtis occidentalis |
| 22840-2409 | Hackberry Pollen | Celtis occidentalis |
| 22840-2410 | Hackberry Pollen | Celtis occidentalis |
| 22840-2411 | Hackberry Pollen | Celtis occidentalis |
| 22840-4445 | Hackberry Pollen | Celtis occidentalis |
| 22840-5429 | Hackberry Pollen | Celtis occidentalis |
| 49643-336 | Hackberry Pollen | Celtis occidentalis |
| 54575-933 | HACKBERRY POLLEN | celtis occidentalis pollen |