22840-1383 : Giant Ragweed 40000 [Pnu]/Ml Intradermal; Percutaneous; Subcutaneous Solution
NDC: | 22840-1383 |
Labeler: | Greer Laboratories, Inc. |
Product Type: | Non-standardized Allergenic |
Drug Name: | Giant Ragweed |
Dosage Form: | Intradermal; Percutaneous; Subcutaneous Solution |
Application #: | BLA101833 |
Rev. Date: |
NDC Package Codes:
- 22840-1383-2: 10 ML IN 1 VIAL, MULTI‑DOSE (22840‑1383‑2)
- 22840-1383-4: 50 ML IN 1 VIAL, MULTI‑DOSE (22840‑1383‑4)
Active Ingredients:
- Ambrosia Trifida Pollen
Dosage Strength:
- 40000 [PNU]/mL
Pharmaceutical Classes:
- Non-Standardized Pollen Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Pollen [CS]
- Allergens [CS]
Related Products:
Based on records with the same trade name.- 22840-1382 Giant Ragweed .1 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
- 22840-1384 Giant Ragweed 20000 [Pnu]/Ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
- 22840-1386 Giant Ragweed .001 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
- 22840-1387 Giant Ragweed .05 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
- 22840-5325 Giant Ragweed .05 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
- 49288-0447 Giant Ragweed .05 g/ml Intradermal; Subcutaneous Injection, Solution by Antigen Laboratories, Inc.
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.