NDC 68071-2222 – Prednisolone Acetate
Prednisolone Acetate 10 mg/mL · Suspension/ Drops · Ophthalmic
Product NDC68071-2222
Product details
- Brand name
- Prednisolone Acetate
- Generic name
- Prednisolone acetate
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- Suspension/ Drops
- Route
- Ophthalmic
- Marketing category
- NDA AUTHORIZED GENERIC · NDA017011
- Marketed since
- August 19, 1997
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 68071-2222-5 | 1 BOTTLE, DROPPER in 1 CARTON (68071-2222-5) / 5 mL in 1 BOTTLE, DROPPER | Jul 27, 2020 |
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