NDC 36987-1210
Flounder
Flounder
Flounder 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 Flounder.
| Product ID | 36987-1210_7c6e2716-24f3-4479-abfc-901a69fc08d9 |
| NDC | 36987-1210 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Flounder |
| Generic Name | Flounder |
| 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 | FLOUNDER |
| 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],Fish Proteins, Dietary [EXT] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 36987-1210-4
50 mL in 1 VIAL, MULTI-DOSE (36987-1210-4)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 36987-1210-2 [36987121002]
Flounder 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 36987-1210-3 [36987121003]
Flounder 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 36987-1210-4 [36987121004]
Flounder 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 36987-1210-1 [36987121001]
Flounder 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 |
|---|---|
| FLOUNDER | .05 g/mL |
OpenFDA Data
| SPL SET ID: | 26081998-16db-41f6-b366-3fd7007b99de |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
Pharmacological Class
- Non-Standardized Food Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Allergens [CS]
- Dietary Proteins [CS]
- Fish Proteins
- Dietary [EXT]
NDC Crossover Matching brand name "Flounder" or generic name "Flounder"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0268-6137 | FLOUNDER | Flounder |
| 22840-5771 | Flounder | Paralichthys lethostigma |
| 36987-1210 | Flounder | Flounder |
| 36987-1211 | Flounder | Flounder |
| 36987-1212 | Flounder | Flounder |
| 36987-1213 | Flounder | Flounder |
| 49288-0200 | Flounder | Flounder |
| 54575-394 | FLOUNDER | flounder |
Trademark Results [Flounder]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 FLOUNDER 88305255 not registered Live/Pending |
BUZZARDS BAY BREWING, INC. 2019-02-18 |
 FLOUNDER 86078200 not registered Dead/Abandoned |
Buzzards Bay Brewing 2013-09-30 |
 FLOUNDER 78189262 3046736 Dead/Cancelled |
Flounder Motor Homes of California LLC 2002-11-26 |
 FLOUNDER 77019642 3292404 Dead/Cancelled |
Gallimore, Keith 2006-10-12 |
 FLOUNDER 73203052 1140369 Dead/Cancelled |
Universal City Studios, Inc. 1979-02-07 |
 FLOUNDER 73203049 1140411 Dead/Cancelled |
Universal City Studios, Inc. 1979-02-07 |
 FLOUNDER 73203048 1147757 Dead/Cancelled |
Universal City Studios, Inc. 1979-02-07 |
 FLOUNDER 73203047 1140432 Dead/Cancelled |
Universal City Studios, Inc. 1979-02-07 |
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