NDC 49288-0169
Dandelion
Dandelion
Dandelion is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Antigen Laboratories, Inc.. The primary component is Taraxacum Officinale Pollen.
| Product ID | 49288-0169_8b59a012-60d1-4fa4-9ee7-fe89524760a2 |
| NDC | 49288-0169 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Dandelion |
| Generic Name | Dandelion |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRADERMAL; SUBCUTANEOUS |
| Marketing Start Date | 1974-03-23 |
| Marketing Category | BLA / BLA |
| Application Number | BLA102223 |
| Labeler Name | Antigen Laboratories, Inc. |
| Substance Name | TARAXACUM OFFICINALE POLLEN |
| Active Ingredient Strength | 0 g/mL |
| Pharm Classes | Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 49288-0169-1
2 mL in 1 VIAL, MULTI-DOSE (49288-0169-1)
| Marketing Start Date | 1974-03-23 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 49288-0169-2 [49288016902]
Dandelion INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0169-4 [49288016904]
Dandelion INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0169-1 [49288016901]
Dandelion INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0169-3 [49288016903]
Dandelion INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0169-5 [49288016905]
Dandelion INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| TARAXACUM OFFICINALE POLLEN | .05 g/mL |
OpenFDA Data
| SPL SET ID: | b8e9933d-eeb3-4379-aaa4-5dfb1179683f |
| Manufacturer | |
| UNII |
|
| RxNorm Concept Unique ID - RxCUI |
Pharmacological Class
- Non-Standardized Pollen Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Increased IgG Production [PE]
- Pollen [CS]
- Allergens [CS]
NDC Crossover Matching brand name "Dandelion" or generic name "Dandelion"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0268-7100 | DANDELION | TARAXACUM OFFICINALE POLLEN |
| 22840-1500 | Dandelion | Taraxacum officinale |
| 22840-1501 | Dandelion | Taraxacum officinale |
| 22840-1502 | Dandelion | Taraxacum officinale |
| 22840-1571 | Dandelion | Taraxacum officinale |
| 22840-1572 | Dandelion | Taraxacum officinale |
| 22840-1573 | Dandelion | Taraxacum officinale |
| 22840-5501 | Dandelion | Taraxacum officinale |
| 36987-3125 | Dandelion | Dandelion |
| 36987-3126 | Dandelion | Dandelion |
| 36987-3127 | Dandelion | Dandelion |
| 36987-3128 | Dandelion | Dandelion |
| 36987-3129 | Dandelion | Dandelion |
| 36987-3130 | Dandelion | Dandelion |
| 36987-3131 | Dandelion | Dandelion |
| 36987-3132 | Dandelion | Dandelion |
| 49288-0169 | Dandelion | Dandelion |
Trademark Results [Dandelion]
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