NDC 17856-0815 – Prednisolone Sodium Phosphate
Prednisolone Sodium Phosphate 15 mg/5mL · Solution · Oral
Product NDC17856-0815
Product details
- Brand name
- Prednisolone Sodium Phosphate
- Generic name
- Prednisolone Sodium Phosphate
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Dosage form
- Solution
- Route
- Oral
- Marketing category
- ANDA · ANDA203559
- Marketed since
- October 9, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Corticosteroid
Active ingredients
- Prednisolone Sodium Phosphate 15 mg/5mL
Uses, dosage, side effects and warnings for PrednisoLONE Sodium Phosphate →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 17856-0815-1 | 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0815-1) / 5 mL in 1 CUP, UNIT-DOSE | Jan 15, 2025 |
| 17856-0815-2 | 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0815-2) / 10 mL in 1 CUP, UNIT-DOSE | Jan 15, 2025 |
| 17856-0815-3 | 48 SYRINGE in 1 BOX, UNIT-DOSE (17856-0815-3) / 5 mL in 1 SYRINGE | Jan 15, 2025 |
| 17856-0815-5 | 45 SYRINGE in 1 BOX, UNIT-DOSE (17856-0815-5) / 5 mL in 1 SYRINGE | Sep 4, 2026 |
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