NDC 54575-366
CAULIFLOWER
Cauliflower
CAULIFLOWER 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 Cauliflower.
| Product ID | 54575-366_dbe7bebd-e445-4e59-8302-e706b795fbde |
| NDC | 54575-366 |
| Product Type | Human Prescription Drug |
| Proprietary Name | CAULIFLOWER |
| Generic Name | Cauliflower |
| 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 | CAULIFLOWER |
| Active Ingredient Strength | 1 g/20mL |
| Pharm Classes | Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Vegetable Proteins [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
Packaging
NDC 54575-366-30
30 mL in 1 VIAL, MULTI-DOSE (54575-366-30)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 54575-366-10 [54575036610]
CAULIFLOWER 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 54575-366-30 [54575036630]
CAULIFLOWER 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 54575-366-02 [54575036602]
CAULIFLOWER 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 54575-366-50 [54575036650]
CAULIFLOWER 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 |
|---|---|
| CAULIFLOWER | 1 g/20mL |
OpenFDA Data
Pharmacological Class
- Non-Standardized Plant Allergenic Extract [EPC]
- Non-Standardized Food Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Allergens [CS]
- Dietary Proteins [CS]
- Plant Proteins [CS]
- Vegetable Proteins [CS]
NDC Crossover Matching brand name "CAULIFLOWER" or generic name "Cauliflower"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 22840-5713 | Cauliflower | Brassica oleracea var. botrytis |
| 36987-1430 | Cauliflower | Cauliflower |
| 36987-1431 | Cauliflower | Cauliflower |
| 36987-1432 | Cauliflower | Cauliflower |
| 36987-1433 | Cauliflower | Cauliflower |
| 49288-0107 | Cauliflower | Cauliflower |
| 54575-366 | CAULIFLOWER | cauliflower |
Trademark Results [CAULIFLOWER]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CAULIFLOWER 77275319 3568323 Dead/Cancelled |
Kabushiki Kaisha Miyake Design Jimusho 2007-09-10 |
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