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: | 49288-9933-5 |
Package Description: | 9 mL in 1 VIAL (49288-9933-5) |
NDC Code | 49288-9933-5 |
Proprietary Name | Sterile Diluent for Allergenic Extract |
Package Description | 9 mL in 1 VIAL (49288-9933-5) |
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 |