NDC 61314-637 – Prednisolone Acetate
Prednisolone Acetate 10 mg/mL · Suspension/ Drops · Ophthalmic
Product NDC61314-637
Product details
- Brand name
- Prednisolone Acetate
- Generic name
- Prednisolone Acetate
- Labeler
- Sandoz Inc
- Dosage form
- Suspension/ Drops
- Route
- Ophthalmic
- Marketing category
- NDA AUTHORIZED GENERIC · NDA017469
- Marketed since
- December 15, 1994
- 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 |
|---|---|---|
| 61314-637-05 | 1 BOTTLE, PLASTIC in 1 CARTON (61314-637-05) / 5 mL in 1 BOTTLE, PLASTIC | Dec 15, 1994 |
| 61314-637-10 | 1 BOTTLE, PLASTIC in 1 CARTON (61314-637-10) / 10 mL in 1 BOTTLE, PLASTIC | Dec 15, 1994 |
| 61314-637-15 | 1 BOTTLE, PLASTIC in 1 CARTON (61314-637-15) / 15 mL in 1 BOTTLE, PLASTIC | Dec 15, 1994 |
Recalls mentioning this NDC
- D-1105-2022 Jun 15, 2022 · Class II
cGMP deviations: Temperature abuse
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