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PREDNISOLONE ACETATE
PREDNISOLONE ACETATE - 60758-119-15 - (prednisolone acetate)
Drug Information of PREDNISOLONE ACETATE
| Product NDC: | 60758-119 |
| 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/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PREDNISOLONE ACETATE
| Product NDC: | 60758-119 |
| Labeler Name: | Pacific Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017011 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19970819 |
Package Information of PREDNISOLONE ACETATE
| Package NDC: | 60758-119-15 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (60758-119-15) > 15 mL in 1 BOTTLE, DROPPER |
NDC Information of PREDNISOLONE ACETATE
| NDC Code | 60758-119-15 |
| Proprietary Name | PREDNISOLONE ACETATE |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (60758-119-15) > 15 mL in 1 BOTTLE, DROPPER |
| Product NDC | 60758-119 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | prednisolone acetate |
| Dosage Form Name | SUSPENSION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19970819 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Pacific Pharma, Inc. |
| Substance Name | PREDNISOLONE ACETATE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
