DATE PALM POLLEN is a Percutaneous; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Allergy Laboratories, Inc.. The primary component is Phoenix Dactylifera Pollen.
Product ID | 54575-959_dbe7bebd-e445-4e59-8302-e706b795fbde |
NDC | 54575-959 |
Product Type | Human Prescription Drug |
Proprietary Name | DATE PALM POLLEN |
Generic Name | Phoenix Dactylifera Pollen |
Dosage Form | Injection, Solution |
Route of Administration | PERCUTANEOUS; SUBCUTANEOUS |
Marketing Start Date | 1967-12-07 |
Marketing Category | BLA / BLA |
Application Number | BLA101376 |
Labeler Name | Allergy Laboratories, Inc. |
Substance Name | PHOENIX DACTYLIFERA POLLEN |
Active Ingredient Strength | 1 g/20mL |
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 | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 1967-12-07 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | BLA |
Application Number | BLA101376 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1967-12-07 |
Inactivation Date | 2020-01-31 |
Marketing Category | BLA |
Application Number | BLA101376 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1967-12-07 |
Inactivation Date | 2020-01-31 |
Marketing Category | BLA |
Application Number | BLA101376 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1967-12-07 |
Inactivation Date | 2020-01-31 |
Marketing Category | BLA |
Application Number | BLA101376 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1967-12-07 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
PHOENIX DACTYLIFERA POLLEN | 1 g/20mL |
NDC | Brand Name | Generic Name |
---|---|---|
49643-387 | Date Palm Pollen | Phoenix dactylifera |
54575-959 | DATE PALM POLLEN | phoenix dactylifera pollen |