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PREDNISOLONE SODIUM PHOSPHATE
PREDNISOLONE SODIUM PHOSPHATE - 24208-715-02 - (PREDNISOLONE SODIUM PHOSPHATE)
Drug Information of PREDNISOLONE SODIUM PHOSPHATE
| Product NDC: | 24208-715 |
| Proprietary Name: | PREDNISOLONE SODIUM PHOSPHATE |
| Non Proprietary Name: | PREDNISOLONE SODIUM PHOSPHATE |
| Active Ingredient(s): | 10 mg/mL & nbsp; PREDNISOLONE SODIUM PHOSPHATE |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PREDNISOLONE SODIUM PHOSPHATE
| Product NDC: | 24208-715 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040070 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19940729 |
Package Information of PREDNISOLONE SODIUM PHOSPHATE
| Package NDC: | 24208-715-02 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (24208-715-02) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of PREDNISOLONE SODIUM PHOSPHATE
| NDC Code | 24208-715-02 |
| Proprietary Name | PREDNISOLONE SODIUM PHOSPHATE |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-715-02) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 24208-715 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PREDNISOLONE SODIUM PHOSPHATE |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19940729 |
| Marketing Category Name | ANDA |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
