Blueberry is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Nelco Laboratories, Inc.. The primary component is Blueberry.
| Product ID | 36987-1304_20425e8b-8db3-4a2b-813b-7e3e1bc1c4e6 |
| NDC | 36987-1304 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Blueberry |
| Generic Name | Blueberry |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRADERMAL; SUBCUTANEOUS |
| Marketing Start Date | 1972-08-29 |
| Marketing Category | BLA / BLA |
| Application Number | BLA102192 |
| Labeler Name | Nelco Laboratories, Inc. |
| Substance Name | BLUEBERRY |
| Active Ingredient Strength | 0 g/mL |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| 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 | 2019-10-21 |
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
| Ingredient | Strength |
|---|---|
| BLUEBERRY | .1 g/mL |
| 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 |