| NDC Code | 24208-715-10 |
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| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-715-10) / 10 mL in 1 BOTTLE, DROPPER |
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| Product NDC | 24208-715 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Prednisolone Sodium Phosphate |
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| Non-Proprietary Name | Prednisolone Sodium Phosphate |
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| Dosage Form | SOLUTION/ DROPS |
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| Usage | OPHTHALMIC |
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| Start Marketing Date | 19940729 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040070 |
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| Manufacturer | Bausch & Lomb Incorporated |
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| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
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| Strength | 10 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
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