Flaxseed 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 Flax Seed.
| Product ID | 49288-0201_afc65820-1d95-4bc6-81a6-ef5ca82cbd81 |
| NDC | 49288-0201 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Flaxseed |
| Generic Name | Flaxseed |
| 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 | FLAX SEED |
| Active Ingredient Strength | 0 g/mL |
| Pharm Classes | Non-Standardized Food Allergenic Extract [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Seed Storage Proteins [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 1974-03-23 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
| Ingredient | Strength |
|---|---|
| FLAX SEED | .05 g/mL |
| SPL SET ID: | 040dacaf-4ccf-425a-9b40-586176b7631d |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 22840-1521 | Flaxseed | Linum usitatissimum |
| 22840-1523 | Flaxseed | Linum usitatissimum |
| 22840-5510 | Flaxseed | Linum usitatissimum |
| 36987-2214 | Flaxseed | Flaxseed |
| 36987-2215 | Flaxseed | Flaxseed |
| 36987-2216 | Flaxseed | Flaxseed |
| 36987-2217 | Flaxseed | Flaxseed |
| 36987-2218 | Flaxseed | Flaxseed |
| 36987-2219 | Flaxseed | Flaxseed |
| 36987-2220 | Flaxseed | Flaxseed |
| 36987-2221 | Flaxseed | Flaxseed |
| 49288-0201 | Flaxseed | Flaxseed |
| 49643-010 | Flaxseed | Flaxseed |