22840-5619 : Fusarium Solani .025 g/ml Intradermal; Percutaneous; Subcutaneous Solution
| NDC: | 22840-5619 |
| Labeler: | Greer Laboratories, Inc. |
| Product Type: | Non-standardized Allergenic |
| Drug Name: | Fusarium Solani |
| Dosage Form: | Intradermal; Percutaneous; Subcutaneous Solution |
| Application #: | BLA101833 |
| Rev. Date: |
NDC Package Codes:
- 22840-5619-2: 10 ML IN 1 VIAL, MULTI‑DOSE (22840‑5619‑2)
- 22840-5619-4: 50 ML IN 1 VIAL, MULTI‑DOSE (22840‑5619‑4)
- 22840-5619-5: 5 ML IN 1 BOTTLE, DROPPER (22840‑5619‑5)
Active Ingredients:
- Haematonectria Haematococca
Dosage Strength:
- .025 g/mL
Pharmaceutical Classes:
- Allergens [CS]
- Cell-mediated Immunity [PE]
- Fungal Proteins [CS]
- Increased Histamine Release [PE]
- Increased IgG Production [PE]
- Non-Standardized Fungal Allergenic Extract [EPC]
Related Products:
Based on records with the same trade name.- 22840-1676 Fusarium Solani .025 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
- 22840-1677 Fusarium Solani 20000 [Pnu]/Ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
- 22840-1678 Fusarium Solani .001 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
- 54575-197 Fusarium Solani 1 g/20ml Percutaneous; Subcutaneous Injection, Solution by Allergy 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.
