NDC 54575-486
PEPPERMINT
Peppermint
PEPPERMINT 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 Peppermint.
| Product ID | 54575-486_dbe7bebd-e445-4e59-8302-e706b795fbde |
| NDC | 54575-486 |
| Product Type | Human Prescription Drug |
| Proprietary Name | PEPPERMINT |
| Generic Name | Peppermint |
| 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 | PEPPERMINT |
| 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],Food Additives [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
Packaging
NDC 54575-486-30
30 mL in 1 VIAL, MULTI-DOSE (54575-486-30)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 54575-486-50 [54575048650]
PEPPERMINT 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 54575-486-02 [54575048602]
PEPPERMINT 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 54575-486-10 [54575048610]
PEPPERMINT 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 54575-486-30 [54575048630]
PEPPERMINT 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 |
|---|---|
| PEPPERMINT | 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]
- Food Additives [CS]
NDC Crossover Matching brand name "PEPPERMINT" or generic name "Peppermint"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 36987-1726 | Peppermint | Peppermint |
| 36987-1727 | Peppermint | Peppermint |
| 36987-1728 | Peppermint | Peppermint |
| 36987-1729 | Peppermint | Peppermint |
| 54575-486 | PEPPERMINT | peppermint |
| 71446-002 | Dr Tans Pain Releiving 3 day Herabl Patch | PEPPERMINT |
| 71960-0002 | GREEN GEMSTONE | peppermint |
| 70470-8003 | Swelling Solution | peppermint |
Trademark Results [PEPPERMINT]
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