COMMON MUGWORT 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 Artemisia Vulgaris Pollen.
Product ID | 54575-136_dbe7bebd-e445-4e59-8302-e706b795fbde |
NDC | 54575-136 |
Product Type | Human Prescription Drug |
Proprietary Name | COMMON MUGWORT POLLEN |
Generic Name | Artemisia Vulgaris 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 | ARTEMISIA VULGARIS POLLEN |
Active Ingredient Strength | 1 g/20mL |
Pharm Classes | Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [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 |
---|---|
ARTEMISIA VULGARIS POLLEN | 1 g/20mL |
NDC | Brand Name | Generic Name |
---|---|---|
54575-136 | COMMON MUGWORT POLLEN | artemisia vulgaris pollen |
0268-0110 | CENTER-AL - ARTEMISIA VULGARIS POLLEN | ARTEMISIA VULGARIS POLLEN |