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NDC 00268-1531-50 AMBROSIA ARTEMISIIFOLIA POLLEN 0.1 g/mL Details
AMBROSIA ARTEMISIIFOLIA POLLEN 0.1 g/mL
AMBROSIA ARTEMISIIFOLIA POLLEN is a SUBCUTANEOUS INJECTION, SOLUTION in the NON-STANDARDIZED ALLERGENIC category. It is labeled and distributed by ALK-Abello, Inc.. The primary component is AMBROSIA ARTEMISIIFOLIA POLLEN.
Product Information
| NDC | 00268-1531 |
|---|---|
| Product ID | 0268-1531_a3200b5f-95f3-43cf-a26f-27a503470956 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | AMBROSIA ARTEMISIIFOLIA POLLEN |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Ragweed Short |
| Product Type | NON-STANDARDIZED ALLERGENIC |
| Dosage Form | INJECTION, SOLUTION |
| Route | SUBCUTANEOUS |
| Active Ingredient Strength | 0.1 |
| Active Ingredient Units | g/mL |
| Substance Name | AMBROSIA ARTEMISIIFOLIA POLLEN |
| Labeler Name | ALK-Abello, Inc. |
| Pharmaceutical Class | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Pollen [CS], Standardized Pollen Allergenic Extract [EPC] |
| DEA Schedule | n/a |
| Marketing Category | BLA |
| Application Number | BLA103753 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00268-1531-50 (00268153150)
| NDC Package Code | 0268-1531-50 |
|---|---|
| Billing NDC | 00268153150 |
| Package | 50 mL in 1 VIAL, MULTI-DOSE (0268-1531-50) |
| Marketing Start Date | 1965-01-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |