Mango 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 Mango.
Product ID | 36987-1595_c9d2ad91-0541-4504-a528-c0cc93a99e4e |
NDC | 36987-1595 |
Product Type | Human Prescription Drug |
Proprietary Name | Mango |
Generic Name | Mango |
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 | MANGO |
Active Ingredient Strength | 0 g/mL |
Pharm Classes | Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Fruit Proteins [EXT] |
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 |
---|---|
MANGO | .05 g/mL |
NDC | Brand Name | Generic Name |
---|---|---|
36987-1594 | Mango | Mango |
36987-1595 | Mango | Mango |
36987-1596 | Mango | Mango |
36987-1597 | Mango | Mango |
57691-566 | Mango | Alcohol |
57691-825 | Mango | Alcohol |