NDC 49288-0591
Vanilla Bean
Vanilla Bean
Vanilla Bean is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Antigen Laboratories, Inc.. The primary component is Vanilla.
| Product ID | 49288-0591_1d11d7ba-8b48-401c-a02e-42b54abb4296 |
| NDC | 49288-0591 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Vanilla Bean |
| Generic Name | Vanilla Bean |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRADERMAL; SUBCUTANEOUS |
| Marketing Start Date | 1974-03-23 |
| Marketing Category | BLA / BLA |
| Application Number | BLA102223 |
| Labeler Name | Antigen Laboratories, Inc. |
| Substance Name | VANILLA |
| Active Ingredient Strength | 0 g/mL |
| Pharm Classes | Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Food Additives [CS],Dietary Proteins [CS],Allergens [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 49288-0591-5
50 mL in 1 VIAL, MULTI-DOSE (49288-0591-5)
| Marketing Start Date | 1974-03-23 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 49288-0591-5 [49288059105]
Vanilla Bean INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0591-4 [49288059104]
Vanilla Bean INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0591-1 [49288059101]
Vanilla Bean INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0591-2 [49288059102]
Vanilla Bean INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0591-3 [49288059103]
Vanilla Bean INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| VANILLA | .05 g/mL |
OpenFDA Data
Pharmacological Class
- Non-Standardized Food Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Food Additives [CS]
- Dietary Proteins [CS]
- Allergens [CS]
NDC Crossover Matching brand name "Vanilla Bean" or generic name "Vanilla Bean"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 49288-0591 | Vanilla Bean | Vanilla Bean |
| 0268-6230 | VANILLA | VANILLA BEAN |
Trademark Results [Vanilla Bean]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VANILLA BEAN 97047832 not registered Live/Pending |
Yao, Linda 2021-09-27 |
 VANILLA BEAN 85656852 4290468 Dead/Cancelled |
John B. Sanfilippo & Son, Inc. 2012-06-20 |
 VANILLA BEAN 85413115 4244444 Dead/Cancelled |
Vanilla Bean Services, Inc. 2011-09-01 |
 VANILLA BEAN 85007632 not registered Dead/Abandoned |
Vanilla Bean Services Inc. 2010-04-06 |
 VANILLA BEAN 85007609 not registered Dead/Abandoned |
Vanilla Bean Services Inc. 2010-04-06 |
 VANILLA BEAN 85007599 not registered Dead/Abandoned |
Vanilla Bean Services Inc. 2010-04-06 |
 VANILLA BEAN 79187073 5211285 Live/Registered |
Grünzeug GmbH 2015-11-27 |
 VANILLA BEAN 75425652 2228344 Dead/Cancelled |
VANILLA BEAN BAKING CORP. 1998-01-29 |
 VANILLA BEAN 74442049 not registered Dead/Abandoned |
Kuma Sport, Inc. 1993-09-29 |
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