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PRED FORTE
PRED FORTE - 54569-0871-0 - (prednisolone acetate)
Drug Information of PRED FORTE
| Product NDC: | 54569-0871 |
| Proprietary Name: | PRED FORTE |
| Non Proprietary Name: | prednisolone acetate |
| Active Ingredient(s): | 10 mg/mL & nbsp; prednisolone acetate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SUSPENSION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PRED FORTE
| Product NDC: | 54569-0871 |
| Labeler Name: | A-S Medication Solutions LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017011 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19730601 |
Package Information of PRED FORTE
| Package NDC: | 54569-0871-0 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (54569-0871-0) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of PRED FORTE
| NDC Code | 54569-0871-0 |
| Proprietary Name | PRED FORTE |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (54569-0871-0) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 54569-0871 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | prednisolone acetate |
| Dosage Form Name | SUSPENSION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19730601 |
| Marketing Category Name | NDA |
| Labeler Name | A-S Medication Solutions LLC |
| Substance Name | PREDNISOLONE ACETATE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
