NDC 54575-390
WHOLE EGG
Egg
WHOLE EGG is a Percutaneous; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Allergy Laboratories, Inc.. The primary component is Egg.
| Product ID | 54575-390_dbe7bebd-e445-4e59-8302-e706b795fbde |
| NDC | 54575-390 |
| Product Type | Human Prescription Drug |
| Proprietary Name | WHOLE EGG |
| Generic Name | Egg |
| Dosage Form | Injection, Solution |
| Route of Administration | PERCUTANEOUS; SUBCUTANEOUS |
| Marketing Start Date | 1972-08-29 |
| Marketing Category | BLA / BLA |
| Application Number | BLA102192 |
| Labeler Name | Allergy Laboratories, Inc. |
| Substance Name | EGG |
| Active Ingredient Strength | 1 g/20mL |
| Pharm Classes | Egg Proteins, Dietary [CS],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
Packaging
NDC 54575-390-30
30 mL in 1 VIAL, MULTI-DOSE (54575-390-30)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 54575-390-30 [54575039030]
WHOLE EGG INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2020-01-31 |
NDC 54575-390-02 [54575039002]
WHOLE EGG INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2020-01-31 |
NDC 54575-390-10 [54575039010]
WHOLE EGG INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2020-01-31 |
NDC 54575-390-50 [54575039050]
WHOLE EGG INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2020-01-31 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| EGG | 1 g/20mL |
OpenFDA Data
Pharmacological Class
- Egg Proteins
- Dietary [CS]
- Non-Standardized Food Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Allergens [CS]
- Dietary Proteins [CS]
NDC Crossover Matching brand name "WHOLE EGG" or generic name "Egg"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 36987-1138 | Whole Egg | Whole Egg |
| 36987-1139 | Whole Egg | Whole Egg |
| 36987-1140 | Whole Egg | Whole Egg |
| 36987-1141 | Whole Egg | Whole Egg |
| 49288-0189 | Whole Egg | Whole Egg |
| 54575-390 | WHOLE EGG | egg |
| 0268-6135 | EGG, WHOLE | EGG |
Trademark Results [WHOLE EGG]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 WHOLE EGG 97275337 not registered Live/Pending |
A-SHA REPUBLIC INC. 2022-02-19 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.