NDC 49288-0055
Blueberry
Blueberry
Blueberry 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 Blueberry.
| Product ID | 49288-0055_1d11d7ba-8b48-401c-a02e-42b54abb4296 |
| NDC | 49288-0055 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Blueberry |
| Generic Name | Blueberry |
| 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 | BLUEBERRY |
| Active Ingredient Strength | 0 g/mL |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 49288-0055-4
30 mL in 1 VIAL, MULTI-DOSE (49288-0055-4)
| Marketing Start Date | 1974-03-23 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 49288-0055-5 [49288005505]
Blueberry 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 49288-0055-3 [49288005503]
Blueberry 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 49288-0055-2 [49288005502]
Blueberry 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 49288-0055-4 [49288005504]
Blueberry 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 49288-0055-1 [49288005501]
Blueberry 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 |
|---|---|
| BLUEBERRY | .05 g/mL |
OpenFDA Data
NDC Crossover Matching brand name "Blueberry" or generic name "Blueberry"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 22840-5707 | Blueberry | Vaccinium myrtilloides |
| 36987-1302 | Blueberry | Blueberry |
| 36987-1303 | Blueberry | Blueberry |
| 36987-1304 | Blueberry | Blueberry |
| 36987-1305 | Blueberry | Blueberry |
| 49288-0055 | Blueberry | Blueberry |
| 54575-354 | BLUEBERRY | blue ridge blueberry |
Trademark Results [Blueberry]
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