Sulfacetamide Sodium and Prednisolone Sodium Phosphate
- Product NDC
- 70518-2559
- 11-digit product format
- 705182559
- Labeler code
- 70518
- Product ID
- 70518-2559_e39dd89b-57ea-323e-e053-2995a90a64c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sulfacetamide Sodium and Prednisolone Sodium Phosphate
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074449
- Marketing category
- ANDA
- Marketing start
- 2020-01-30
- Marketing end
- 0000-00-00
- Substance
- PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM
- Active strength
- 2 mg/mL; mg/mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Sulfonamide Antibacterial [EPC], Sulfonamides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2559-0 | 70518255900 | 1 BOTTLE, DROPPER in 1 CARTON (70518-2559-0) > 5 mL in 1 BOTTLE, DROPPER | 2020-01-30 | 0000-00-00 | No | No | Current |