NDC 36987-1371
Strawberry
Strawberry
Strawberry is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Nelco Laboratories, Inc.. The primary component is Strawberry.
| Product ID | 36987-1371_c9d2ad91-0541-4504-a528-c0cc93a99e4e |
| NDC | 36987-1371 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Strawberry |
| Generic Name | Strawberry |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRADERMAL; SUBCUTANEOUS |
| Marketing Start Date | 1972-08-29 |
| Marketing Category | BLA / BLA |
| Application Number | BLA102192 |
| Labeler Name | Nelco Laboratories, Inc. |
| Substance Name | STRAWBERRY |
| Active Ingredient Strength | 0 g/mL |
| Pharm Classes | Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Fruit Proteins [EXT] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 36987-1371-2
10 mL in 1 VIAL, MULTI-DOSE (36987-1371-2)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 36987-1371-3 [36987137103]
Strawberry INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
NDC 36987-1371-1 [36987137101]
Strawberry INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
NDC 36987-1371-2 [36987137102]
Strawberry INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
NDC 36987-1371-4 [36987137104]
Strawberry INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| STRAWBERRY | .05 g/mL |
OpenFDA Data
Pharmacological Class
- Non-Standardized Food Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Allergens [CS]
- Dietary Proteins [CS]
- Fruit Proteins [EXT]
NDC Crossover Matching brand name "Strawberry" or generic name "Strawberry"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0268-6220 | STRAWBERRY | STRAWBERRY |
| 22840-5752 | Strawberry | Fragaria X ananassa |
| 36987-1370 | Strawberry | Strawberry |
| 36987-1371 | Strawberry | Strawberry |
| 36987-1372 | Strawberry | Strawberry |
| 36987-1373 | Strawberry | Strawberry |
| 49288-0480 | Strawberry | Strawberry |
| 54575-462 | STRAWBERRY | strawberry |
Trademark Results [Strawberry]
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.