NDC 36987-2814
Mulberry
Mulberry
Mulberry 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 Broussonetia Papyrifera Pollen.
| Product ID | 36987-2814_c0bd3ba3-a5f1-48f1-a8c2-ab5fefa5f5e6 |
| NDC | 36987-2814 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Mulberry |
| Generic Name | Mulberry |
| 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 | BROUSSONETIA PAPYRIFERA POLLEN |
| Active Ingredient Strength | 10000 [PNU]/mL |
| Pharm Classes | Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 36987-2814-4
50 mL in 1 VIAL, MULTI-DOSE (36987-2814-4)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 36987-2814-2 [36987281402]
Mulberry INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
NDC 36987-2814-3 [36987281403]
Mulberry INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
NDC 36987-2814-4 [36987281404]
Mulberry INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
NDC 36987-2814-1 [36987281401]
Mulberry INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| BROUSSONETIA PAPYRIFERA POLLEN | 10000 [PNU]/mL |
OpenFDA Data
Pharmacological Class
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Increased IgG Production [PE]
- Pollen [CS]
- Allergens [CS]
- Non-Standardized Pollen Allergenic Extract [EPC]
NDC Crossover Matching brand name "Mulberry" or generic name "Mulberry"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 36987-2813 | Mulberry | Mulberry |
| 36987-2814 | Mulberry | Mulberry |
| 36987-2815 | Mulberry | Mulberry |
| 36987-2816 | Mulberry | Mulberry |
| 36987-2817 | Mulberry | Mulberry |
| 36987-2818 | Mulberry | Mulberry |
| 36987-2819 | Mulberry | Mulberry |
| 36987-2820 | Mulberry | Mulberry |
Trademark Results [Mulberry]
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