| NDC Code | 54575-085-50 |
|---|
| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (54575-085-50) |
|---|
| Product NDC | 54575-085 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Annual Bluegrass Pollen |
|---|
| Non-Proprietary Name | Poa Annua Pollen |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | PERCUTANEOUS; SUBCUTANEOUS |
|---|
| Start Marketing Date | 19671207 |
|---|
| Marketing Category Name | BLA |
|---|
| Application Number | BLA101376 |
|---|
| Manufacturer | Allergy Laboratories, Inc. |
|---|
| Substance Name | POA ANNUA POLLEN |
|---|
| Strength | 1 |
|---|
| Strength Unit | g/20mL |
|---|
| Pharmacy Classes | Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS] |
|---|