61786-154 : Sulfacetamide Sodium and Prednisolone Sodium Phosphate Ophthalmic Solution/ Drops


NDC: 61786-154
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name: Sulfacetamide Sodium and Prednisolone Sodium Phosphate
Dosage Form: Ophthalmic Solution/ Drops
Application #: ANDA074449
Rev. Date: 


NDC Package Codes:

  • 61786-154-57: 5 ML IN 1 BOTTLE, DROPPER (61786‑154‑57)

Active Ingredients:

  • Prednisolone Sodium Phosphate
  • Sulfacetamide Sodium

Dosage Strength:

  • 2.3 mg/mL
  • 100 mg/mL

Pharmaceutical Classes:

  • Corticosteroid [EPC]
  • Corticosteroid Hormone Receptor Agonists [MoA]
  • Sulfonamide Antibacterial [EPC]
  • Sulfonamides [Chemical/Ingredient]

Related Products:

Based on records with the same trade name.
  • 61786-738 Sulfacetamide Sodium and Prednisolone Sodium Phosphate Ophthalmic Solution/ Drops by Remedyrepack Inc.
  • 70518-2559 Sulfacetamide Sodium and Prednisolone Sodium Phosphate Ophthalmic Solution/ Drops by Remedyrepack Inc.
  • 21695-186 Sulfacetamide Sodium and Prednisolone Sodium Phosphate Ophthalmic Solution by Rebel Distributors Corp
  • 24208-317 Sulfacetamide Sodium and Prednisolone Sodium Phosphate Ophthalmic Solution/ Drops by Bausch & Lomb Incoporated
  • 53002-8690 Sulfacetamide Sodium and Prednisolone Sodium Phosphate Ophthalmic Solution/ Drops by Rpk Pharmaceuticals, Inc.
  • 61314-297 Sulfacetamide Sodium and Prednisolone Sodium Phosphate Ophthalmic Solution by Falcon Pharmaceuticals, Ltd.
  • 68071-1650 Sulfacetamide Sodium and Prednisolone Sodium Phosphate Ophthalmic Solution/ Drops by Nucare Pharmaceuticals, 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.