NDC 54575-444
SWEET POTATO
Sweet Potato
SWEET POTATO is a Percutaneous; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Allergy Laboratories, Inc.. The primary component is Sweet Potato.
| Product ID | 54575-444_dbe7bebd-e445-4e59-8302-e706b795fbde |
| NDC | 54575-444 |
| Product Type | Human Prescription Drug |
| Proprietary Name | SWEET POTATO |
| Generic Name | Sweet Potato |
| Dosage Form | Injection, Solution |
| Route of Administration | PERCUTANEOUS; SUBCUTANEOUS |
| Marketing Start Date | 1972-08-29 |
| Marketing Category | BLA / BLA |
| Application Number | BLA102192 |
| Labeler Name | Allergy Laboratories, Inc. |
| Substance Name | SWEET POTATO |
| Active Ingredient Strength | 1 g/20mL |
| Pharm Classes | Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Vegetable Proteins [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
Packaging
NDC 54575-444-02
2 mL in 1 VIAL, MULTI-DOSE (54575-444-02)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 54575-444-10 [54575044410]
SWEET POTATO INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2020-01-31 |
NDC 54575-444-30 [54575044430]
SWEET POTATO INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2020-01-31 |
NDC 54575-444-50 [54575044450]
SWEET POTATO INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2020-01-31 |
NDC 54575-444-02 [54575044402]
SWEET POTATO INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2020-01-31 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| SWEET POTATO | 1 g/20mL |
OpenFDA Data
Pharmacological Class
- Non-Standardized Food Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Allergens [CS]
- Dietary Proteins [CS]
- Vegetable Proteins [CS]
NDC Crossover Matching brand name "SWEET POTATO" or generic name "Sweet Potato"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0268-6205 | SWEET POTATO | SWEET POTATO |
| 22840-5743 | Sweet Potato | Ipomoea batatas |
| 36987-1486 | Sweet Potato | Sweet Potato |
| 36987-1487 | Sweet Potato | Sweet Potato |
| 36987-1488 | Sweet Potato | Sweet Potato |
| 36987-1489 | Sweet Potato | Sweet Potato |
| 49288-0388 | Sweet Potato | Sweet Potato |
| 54575-444 | SWEET POTATO | sweet potato |
Trademark Results [SWEET POTATO]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SWEET POTATO 77185590 not registered Dead/Abandoned |
Jacob Birnbaum 2007-05-21 |
 SWEET POTATO 76485049 not registered Dead/Abandoned |
Sweet Potato Baby Food, Inc. 2003-01-27 |
 SWEET POTATO 73221398 1160895 Dead/Cancelled |
Sweet Potato, Inc. 1979-06-27 |
 SWEET POTATO 73085176 1053001 Dead/Cancelled |
Ram Golf Corporation 1976-04-26 |
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