NDC 70748-332 – Prednisolone Acetate
Prednisolone Acetate 10 mg/mL · Suspension/ Drops · Ophthalmic
Product NDC70748-332
Product details
- Brand name
- Prednisolone Acetate
- Generic name
- Prednisolone acetate
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Suspension/ Drops
- Route
- Ophthalmic
- Marketing category
- ANDA · ANDA216935
- Marketed since
- October 11, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Corticosteroid
Active ingredients
- Prednisolone Acetate 10 mg/mL
Uses, dosage, side effects and warnings for Prednisolone Acetate →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70748-332-02 | 1 BOTTLE in 1 CARTON (70748-332-02) / 5 mL in 1 BOTTLE | Oct 11, 2024 |
| 70748-332-03 | 1 BOTTLE in 1 CARTON (70748-332-03) / 10 mL in 1 BOTTLE | Oct 11, 2024 |
| 70748-332-04 | 1 BOTTLE in 1 CARTON (70748-332-04) / 15 mL in 1 BOTTLE | Oct 11, 2024 |
Recalls mentioning this NDC
- D-0655-2026 Jul 8, 2026 · Class II
Presence of Foreign Substance
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