NDC 36987-1314
Cranberry
Cranberry
Cranberry 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 Cranberry.
| Product ID | 36987-1314_dec580ea-73db-4658-9de1-440c19bb42b7 |
| NDC | 36987-1314 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Cranberry |
| Generic Name | Cranberry |
| 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 | CRANBERRY |
| Active Ingredient Strength | 0 g/mL |
| Pharm Classes | Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Non-Standardized Food Allergenic Extract [EPC],Fruit Proteins [EXT] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 36987-1314-1
5 mL in 1 VIAL, MULTI-DOSE (36987-1314-1)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 36987-1314-3 [36987131403]
Cranberry 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 36987-1314-2 [36987131402]
Cranberry 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 36987-1314-1 [36987131401]
Cranberry 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 36987-1314-4 [36987131404]
Cranberry 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 |
|---|---|
| CRANBERRY | .05 g/mL |
OpenFDA Data
Pharmacological Class
- Non-Standardized Plant Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Allergens [CS]
- Dietary Proteins [CS]
- Plant Proteins [CS]
- Non-Standardized Food Allergenic Extract [EPC]
- Fruit Proteins [EXT]
NDC Crossover Matching brand name "Cranberry" or generic name "Cranberry"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 22840-5720 | Cranberry | Vaccinium macrocarpon |
| 36987-1314 | Cranberry | Cranberry |
| 36987-1315 | Cranberry | Cranberry |
| 36987-1316 | Cranberry | Cranberry |
| 36987-1317 | Cranberry | Cranberry |
| 49288-0117 | Cranberry | Cranberry |
| 54575-383 | CRANBERRY | cranberry |
Trademark Results [Cranberry]
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.