BLUEBERRY 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 Blue Ridge Blueberry.
Product ID | 54575-354_dbe7bebd-e445-4e59-8302-e706b795fbde |
NDC | 54575-354 |
Product Type | Human Prescription Drug |
Proprietary Name | BLUEBERRY |
Generic Name | Blue Ridge Blueberry |
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 | BLUE RIDGE BLUEBERRY |
Active Ingredient Strength | 1 g/20mL |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 1972-08-29 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | BLA |
Application Number | BLA102192 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1972-08-29 |
Inactivation Date | 2020-01-31 |
Marketing Category | BLA |
Application Number | BLA102192 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1972-08-29 |
Inactivation Date | 2020-01-31 |
Marketing Category | BLA |
Application Number | BLA102192 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1972-08-29 |
Inactivation Date | 2020-01-31 |
Marketing Category | BLA |
Application Number | BLA102192 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1972-08-29 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
BLUE RIDGE BLUEBERRY | 1 g/20mL |
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 |