NDC 22840-1376
Desert Ragweed
Ambrosia Dumosa
Desert Ragweed is a Intradermal; Percutaneous; Subcutaneous Solution in the Non-standardized Allergenic category. It is labeled and distributed by Greer Laboratories, Inc.. The primary component is Ambrosia Dumosa Pollen.
Product ID | 22840-1376_7b43b65a-bbff-133f-e053-2991aa0a3395 |
NDC | 22840-1376 |
Product Type | Non-standardized Allergenic |
Proprietary Name | Desert Ragweed |
Generic Name | Ambrosia Dumosa |
Dosage Form | Solution |
Route of Administration | INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS |
Marketing Start Date | 1981-09-15 |
Marketing Category | BLA / BLA |
Application Number | BLA101833 |
Labeler Name | Greer Laboratories, Inc. |
Substance Name | AMBROSIA DUMOSA POLLEN |
Active Ingredient Strength | 0 g/mL |
Pharm Classes | Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [CS],Allergens [CS] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |