NDC product
9 TREE MIX
NDC 0268-8022 · ALK-Abello, Inc.
Key facts
| Product NDC | 0268-8022 |
|---|---|
| Proprietary name | 9 TREE MIX |
| Nonproprietary name | ACER SACCHARUM POLLEN, ALNUS RHOMBIFOLIA POLLEN, BETULA LENTA POLLEN, CARYA OVATA POLLEN, FRAXINUS AMERICANA POLLEN, PLATANUS OCCIDENTALIS POLLEN, POPULUS ALBA POLLEN, QUERCUS ALBA POLLEN and ULMUS CRASSIFOLIA POLLEN |
| Substances | ALNUS RHOMBIFOLIA POLLEN, FRAXINUS AMERICANA POLLEN, ULMUS CRASSIFOLIA POLLEN, BETULA LENTA POLLEN, ACER SACCHARUM POLLEN, CARYA OVATA POLLEN, QUERCUS ALBA POLLEN, POPULUS ALBA POLLEN, PLATANUS OCCIDENTALIS POLLEN |
| Dosage form | INJECTION, SOLUTION |
| Route | SUBCUTANEOUS |
| Labeler | ALK-Abello, Inc. |
| Product type | NON-STANDARDIZED ALLERGENIC |
| Marketing category | BLA |
| Application number | BLA103753 |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Pollen Allergenic Extract [EPC], Pollen [CS] |
| Marketing start | Feb 23, 1998 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: