NDC 49288-0114
Cinnamon
Cinnamon
Cinnamon 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 Cinnamon.
| Product ID | 49288-0114_1d11d7ba-8b48-401c-a02e-42b54abb4296 |
| NDC | 49288-0114 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Cinnamon |
| Generic Name | Cinnamon |
| 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 | CINNAMON |
| Active Ingredient Strength | 0 g/mL |
| Pharm Classes | Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Dietary Proteins [CS],Food Additives [CS],Allergens [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 49288-0114-5
50 mL in 1 VIAL, MULTI-DOSE (49288-0114-5)
| Marketing Start Date | 1974-03-23 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 49288-0114-2 [49288011402]
Cinnamon 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 49288-0114-4 [49288011404]
Cinnamon 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 49288-0114-3 [49288011403]
Cinnamon 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 49288-0114-5 [49288011405]
Cinnamon 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 49288-0114-1 [49288011401]
Cinnamon 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 |
|---|---|
| CINNAMON | .05 g/mL |
OpenFDA Data
Pharmacological Class
- Non-Standardized Food Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Dietary Proteins [CS]
- Food Additives [CS]
- Allergens [CS]
NDC Crossover Matching brand name "Cinnamon" or generic name "Cinnamon"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0268-6123 | CINNAMON | CINNAMON |
| 22840-5717 | Cinnamon | Cinnamomum verum |
| 36987-1674 | Cinnamon | Cinnamon |
| 36987-1675 | Cinnamon | Cinnamon |
| 36987-1676 | Cinnamon | Cinnamon |
| 36987-1677 | Cinnamon | Cinnamon |
| 49288-0114 | Cinnamon | Cinnamon |
| 54575-374 | CINNAMON | cinnamon |
| 0220-1406 | Cinnamomum | CINNAMON |
| 68428-322 | Cinnamomum | CINNAMON |
| 71919-204 | Cinnamomum | CINNAMON |
Trademark Results [Cinnamon]
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.