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Prednisolone Acetate
Prednisolone Acetate - 61314-637-15 - (Prednisolone Acetate)
Drug Information of Prednisolone Acetate
| Product NDC: | 61314-637 |
| Proprietary Name: | Prednisolone Acetate |
| Non Proprietary Name: | Prednisolone Acetate |
| Active Ingredient(s): | 10 mg/mL & nbsp; Prednisolone Acetate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prednisolone Acetate
| Product NDC: | 61314-637 |
| Labeler Name: | Falcon Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017469 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19941215 |
Package Information of Prednisolone Acetate
| Package NDC: | 61314-637-15 |
| Package Description: | 15 mL in 1 BOTTLE, PLASTIC (61314-637-15) |
NDC Information of Prednisolone Acetate
| NDC Code | 61314-637-15 |
| Proprietary Name | Prednisolone Acetate |
| Package Description | 15 mL in 1 BOTTLE, PLASTIC (61314-637-15) |
| Product NDC | 61314-637 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Prednisolone Acetate |
| Dosage Form Name | SUSPENSION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19941215 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Falcon Pharmaceuticals |
| Substance Name | PREDNISOLONE ACETATE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
