NDC 54575-358
BUCKWHEAT
Buckwheat
BUCKWHEAT 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 Buckwheat.
| Product ID | 54575-358_dbe7bebd-e445-4e59-8302-e706b795fbde |
| NDC | 54575-358 |
| Product Type | Human Prescription Drug |
| Proprietary Name | BUCKWHEAT |
| Generic Name | Buckwheat |
| 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 | BUCKWHEAT |
| Active Ingredient Strength | 1 g/20mL |
| Pharm Classes | Dietary Proteins [CS],Grain Proteins [EXT],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
Packaging
NDC 54575-358-02
2 mL in 1 VIAL, MULTI-DOSE (54575-358-02)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 54575-358-10 [54575035810]
BUCKWHEAT 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 54575-358-02 [54575035802]
BUCKWHEAT 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 54575-358-50 [54575035850]
BUCKWHEAT 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 54575-358-30 [54575035830]
BUCKWHEAT 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 |
|---|---|
| BUCKWHEAT | 1 g/20mL |
OpenFDA Data
Pharmacological Class
- Dietary Proteins [CS]
- Grain Proteins [EXT]
- Non-Standardized Food Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Allergens [CS]
NDC Crossover Matching brand name "BUCKWHEAT" or generic name "Buckwheat"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0268-6113 | BUCKWHEAT | Buckwheat |
| 22840-5709 | Buckwheat | Fagopyrum esculentum |
| 49288-0051 | Buckwheat | Buckwheat |
| 54575-358 | BUCKWHEAT | buckwheat |
Trademark Results [BUCKWHEAT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BUCKWHEAT 78872545 not registered Dead/Abandoned |
The Cheesecake Café, Inc. 2006-04-28 |
 BUCKWHEAT 78374430 not registered Dead/Abandoned |
KING WORLD PRODUCTIONS INC. 2004-02-26 |
 BUCKWHEAT 78374289 not registered Dead/Abandoned |
KING WORLD PRODUCTIONS INC. 2004-02-26 |
 BUCKWHEAT 78373586 not registered Dead/Abandoned |
KING WORLD PRODUCTIONS INC. 2004-02-25 |
 BUCKWHEAT 78373454 not registered Dead/Abandoned |
KING WORLD PRODUCTIONS INC. 2004-02-24 |
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