NDC 54575-442
POPPY SEED
Poppy Seed
POPPY SEED 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 Poppy Seed.
| Product ID | 54575-442_dbe7bebd-e445-4e59-8302-e706b795fbde |
| NDC | 54575-442 |
| Product Type | Human Prescription Drug |
| Proprietary Name | POPPY SEED |
| Generic Name | Poppy Seed |
| 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 | POPPY SEED |
| Active Ingredient Strength | 1 g/20mL |
| Pharm Classes | Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Seed Storage Proteins [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
Packaging
NDC 54575-442-10
10 mL in 1 VIAL, MULTI-DOSE (54575-442-10)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 54575-442-02 [54575044202]
POPPY SEED 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 54575-442-10 [54575044210]
POPPY SEED 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 54575-442-50 [54575044250]
POPPY SEED 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 54575-442-30 [54575044230]
POPPY SEED 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 |
|---|---|
| POPPY SEED | 1 g/20mL |
OpenFDA Data
Pharmacological Class
- Non-Standardized Plant Allergenic Extract [EPC]
- Non-Standardized Food Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Allergens [CS]
- Dietary Proteins [CS]
- Plant Proteins [CS]
- Seed Storage Proteins [CS]
Trademark Results [POPPY SEED]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 POPPY SEED 73320100 not registered Dead/Abandoned |
HOME LIKE FOOD SPECIALTIES, INC. 1981-07-21 |
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