66758-070 : Maxitrol Ophthalmic Ointment
| NDC: | 66758-070 |
| Labeler: | Sandoz Inc |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Maxitrol |
| Dosage Form: | Ophthalmic Ointment |
| Application #: | NDA050065 |
| Rev. Date: |
NDC Package Codes:
- 66758-070-38: 3.5 G IN 1 TUBE (66758‑070‑38)
Active Ingredients:
- Dexamethasone
- Neomycin Sulfate
- Polymyxin B Sulfate
Dosage Strength:
- 1 mg/g
- 3.5 mg/g
- 10000 [USP'U]/g
Pharmaceutical Classes:
- Aminoglycoside Antibacterial [EPC]
- Aminoglycosides [CS]
- Corticosteroid Hormone Receptor Agonists [MoA]
- Corticosteroid [EPC]
- Polymyxin-class Antibacterial [EPC]
- Polymyxins [CS]
Related Products:
Based on records with the same trade name.- 0065-0631 Maxitrol Ophthalmic Ointment by Alcon Laboratories, Inc.
- 0078-0771 Maxitrol Ophthalmic Ointment by Novartis Pharmaceuticals Corporation
- 0078-0792 Maxitrol Ophthalmic Suspension by Novartis Pharmaceuticals Corporation
- 0998-0630 Maxitrol Ophthalmic Suspension by Alcon Laboratories, Inc.
- 82667-100 Maxitrol Ophthalmic Suspension by Harrow Eye, LLC
NDC QR Code
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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.