| NDC Code | 49643-355-50 |
|---|
| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (49643-355-50) |
|---|
| Product NDC | 49643-355 |
|---|
| Product Type Name | NON-STANDARDIZED ALLERGENIC |
|---|
| Proprietary Name | Desert Ragweed Pollen |
|---|
| Non-Proprietary Name | Ambrosia Dumosa |
|---|
| Dosage Form | INJECTION |
|---|
| Usage | CUTANEOUS; INTRADERMAL; SUBCUTANEOUS |
|---|
| Start Marketing Date | 19740312 |
|---|
| Marketing Category Name | BLA |
|---|
| Application Number | BLA102211 |
|---|
| Manufacturer | Allermed Laboratories, Inc. |
|---|
| Substance Name | AMBROSIA DUMOSA POLLEN |
|---|
| Strength | .05 |
|---|
| Strength Unit | g/mL |
|---|
| Pharmacy Classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Non-Standardized Pollen Allergenic Extract [EPC], Pollen [CS] |
|---|