NDC product
9 TREE MIX
NDC 0268-8021 · ALK-Abello, Inc.
Key facts
| Product NDC | 0268-8021 |
|---|---|
| Proprietary name | 9 TREE MIX |
| Nonproprietary name | ACER SACCHARINUM POLLEN, ALNUS RHOMBIFOLIA POLLEN, BETULA LENTA WHOLE, CARYA OVATA POLLEN, FRAXINUS AMERICANA POLLEN, PLATANUS OCCIDENTALIS POLLEN, POPULUS ALBA POLLEN, QUERCUS ALBA POLLEN, ULMUS CRASSIFOLIA POLLEN |
| Substances | ALNUS RHOMBIFOLIA POLLEN, FRAXINUS AMERICANA POLLEN, ULMUS CRASSIFOLIA POLLEN, BETULA LENTA WHOLE, ACER SACCHARINUM 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 | Jan 1, 1965 |
| 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: