NDC 36987-1505
Rhubarb
Rhubarb
Rhubarb 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 Rhubarb.
| Product ID | 36987-1505_255e0c54-6613-460b-a91f-452fdfd0319d |
| NDC | 36987-1505 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Rhubarb |
| Generic Name | Rhubarb |
| 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 | RHUBARB |
| Active Ingredient Strength | 0 g/mL |
| Pharm Classes | Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 36987-1505-4
50 mL in 1 VIAL, MULTI-DOSE (36987-1505-4)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 36987-1505-1 [36987150501]
Rhubarb 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 36987-1505-2 [36987150502]
Rhubarb 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 36987-1505-4 [36987150504]
Rhubarb 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 36987-1505-3 [36987150503]
Rhubarb 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 |
|---|---|
| RHUBARB | .1 g/mL |
OpenFDA Data
Pharmacological Class
- Non-Standardized Plant Allergenic Extract [EPC]
- Non-Standardized Food Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Allergens [CS]
- Dietary Proteins [CS]
- Plant Proteins [CS]
NDC Crossover Matching brand name "Rhubarb" or generic name "Rhubarb"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 36987-1502 | Rhubarb | Rhubarb |
| 36987-1503 | Rhubarb | Rhubarb |
| 36987-1504 | Rhubarb | Rhubarb |
| 36987-1505 | Rhubarb | Rhubarb |
| 54575-451 | RHUBARB | rhubarb |
Trademark Results [Rhubarb]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 RHUBARB 98511599 not registered Live/Pending |
Rhubarb Labs Inc. 2024-04-22 |
 RHUBARB 86692155 4901547 Live/Registered |
RHUBARB LLC 2015-07-14 |
 RHUBARB 86566388 4904032 Live/Registered |
Ramoth Group, LLC 2015-03-17 |
 RHUBARB 85034330 not registered Dead/Abandoned |
Those Characters From Cleveland, Inc. 2010-05-10 |
 RHUBARB 79196373 5450524 Live/Registered |
H.A.G. Import Corpn. (Australia) Pty Ltd 2016-03-10 |
 RHUBARB 79074767 not registered Dead/Abandoned |
H.A.G. Import Corpn. (Australia) Pty Ltd 2009-06-11 |
 RHUBARB 79000205 2942223 Dead/Cancelled |
Rhubarb Enterprises Pty Ltd 2003-12-05 |
 RHUBARB 76068554 2840593 Dead/Cancelled |
THOSE CHARACTERS FROM CLEVELAND, INC. 2000-06-12 |
 RHUBARB 74062849 not registered Dead/Abandoned |
Those Characters From Cleveland, Inc. 1990-05-25 |
 RHUBARB 73341763 1238279 Dead/Cancelled |
American Greetings Corporation 1981-12-14 |
 RHUBARB 71439563 0387089 Dead/Cancelled |
PEGGY SAGE, INC. 1941-01-10 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.