| Product NDC: | 49288-9933 |
| Proprietary Name: | Sterile Diluent for Allergenic Extract |
| Non Proprietary Name: | Phenol |
| Active Ingredient(s): | .004 mL/mL & nbsp; Phenol |
| Administration Route(s): | INTRADERMAL; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49288-9933 |
| Labeler Name: | Antigen Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA102223 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19740323 |
| Package NDC: | 49288-9933-7 |
| Package Description: | 30 mL in 1 VIAL (49288-9933-7) |
| NDC Code | 49288-9933-7 |
| Proprietary Name | Sterile Diluent for Allergenic Extract |
| Package Description | 30 mL in 1 VIAL (49288-9933-7) |
| Product NDC | 49288-9933 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenol |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRADERMAL; SUBCUTANEOUS |
| Start Marketing Date | 19740323 |
| Marketing Category Name | BLA |
| Labeler Name | Antigen Laboratories, Inc. |
| Substance Name | PHENOL |
| Strength Number | .004 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |