22840-5774 : Oyster .05 g/ml Intradermal; Percutaneous; Subcutaneous Solution
| NDC: | 22840-5774 |
| Labeler: | Greer Laboratories, Inc. |
| Product Type: | Non-standardized Allergenic |
| Drug Name: | Oyster |
| Dosage Form: | Intradermal; Percutaneous; Subcutaneous Solution |
| Application #: | BLA101833 |
| Rev. Date: |
NDC Package Codes:
- 22840-5774-2: 10 ML IN 1 VIAL, MULTI‑DOSE (22840‑5774‑2)
- 22840-5774-5: 5 ML IN 1 BOTTLE, DROPPER (22840‑5774‑5)
Active Ingredients:
- Eastern Oyster
Dosage Strength:
- .05 g/mL
Related Products:
Based on records with the same trade name.- 0268-6189 Oyster .1 g/ml Percutaneous Injection, Solution by Alk-abello, Inc.
- 36987-1234 Oyster .05 g/ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
- 36987-1235 Oyster .05 g/ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
- 36987-1236 Oyster .1 g/ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
- 36987-1237 Oyster .1 g/ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
- 49288-0336 Oyster .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.
