Blackberry 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 Blackberry.
Product ID | 36987-1299_c9d2ad91-0541-4504-a528-c0cc93a99e4e |
NDC | 36987-1299 |
Product Type | Human Prescription Drug |
Proprietary Name | Blackberry |
Generic Name | Blackberry |
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 | BLACKBERRY |
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 |
---|---|
BLACKBERRY | .05 g/mL |
NDC | Brand Name | Generic Name |
---|---|---|
36987-1298 | Blackberry | Blackberry |
36987-1299 | Blackberry | Blackberry |
36987-1300 | Blackberry | Blackberry |
36987-1301 | Blackberry | Blackberry |
49288-0054 | Blackberry | Blackberry |
54575-353 | BLACKBERRY | blackberry |