| NDC Code | 49288-0591-5 |
|---|
| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (49288-0591-5) |
|---|
| Product NDC | 49288-0591 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Vanilla Bean |
|---|
| Non-Proprietary Name | Vanilla Bean |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | INTRADERMAL; SUBCUTANEOUS |
|---|
| Start Marketing Date | 19740323 |
|---|
| Marketing Category Name | BLA |
|---|
| Application Number | BLA102223 |
|---|
| Manufacturer | Antigen Laboratories, Inc. |
|---|
| Substance Name | VANILLA |
|---|
| Strength | .05 |
|---|
| Strength Unit | g/mL |
|---|
| Pharmacy Classes | Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Food Additives [CS],Dietary Proteins [CS],Allergens [CS] |
|---|