0065-0638 : Omnipred 10 mg/ml Ophthalmic Suspension
| NDC: | 0065-0638 |
| Labeler: | Alcon Laboratories, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Omnipred |
| Dosage Form: | Ophthalmic Suspension |
| Application #: | NDA017469 |
| Rev. Date: |
NDC Package Codes:
- 0065-0638-25: 10 ML IN 1 BOTTLE, PLASTIC (0065‑0638‑25)
- 0065-0638-27: 5 ML IN 1 BOTTLE, PLASTIC (0065‑0638‑27)
Active Ingredients:
- Prednisolone Acetate
Dosage Strength:
- 10 mg/mL
Pharmaceutical Classes:
- Corticosteroid [EPC]
- Corticosteroid Hormone Receptor Agonists [MoA]
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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.