FDA NDC Directory · JSON-LD · Markdown
NDC 49643-501 · NON-STANDARDIZED ALLERGENIC · LIQUID
| Generic name | Alnus rhombifolia/Alnus rubra/Alnus rugosa |
|---|---|
| Labeler / Manufacturer | Allermed Laboratories, Inc. |
| Marketing category | Biologic License Application · App BLA102211 |
| Dosage form / route | LIQUID · PERCUTANEOUS SUBCUTANEOUS |
| Active ingredients | ALNUS INCANA SUBSP. RUGOSA POLLEN (.0167 g/mL) ALNUS RHOMBIFOLIA POLLEN (.0167 g/mL) ALNUS RUBRA POLLEN (.0167 g/mL) |
| Marketing started | 19740312 |
| Package count | 4 |
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