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Dexamethasone Sodium Phosphate
Dexamethasone Sodium Phosphate - 57319-065-01 - (Dexamethasone Sodium Phosphate)
Drug Information of Dexamethasone Sodium Phosphate
| Product NDC: | 57319-065 |
| Proprietary Name: | Dexamethasone Sodium Phosphate |
| Non Proprietary Name: | Dexamethasone Sodium Phosphate |
| Active Ingredient(s): | 1 mg/mL & nbsp; Dexamethasone Sodium Phosphate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dexamethasone Sodium Phosphate
| Product NDC: | 57319-065 |
| Labeler Name: | Phoenix Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040069 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960726 |
Package Information of Dexamethasone Sodium Phosphate
| Package NDC: | 57319-065-01 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (57319-065-01) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of Dexamethasone Sodium Phosphate
| NDC Code | 57319-065-01 |
| Proprietary Name | Dexamethasone Sodium Phosphate |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (57319-065-01) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 57319-065 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dexamethasone Sodium Phosphate |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19960726 |
| Marketing Category Name | ANDA |
| Labeler Name | Phoenix Pharmaceutical, Inc. |
| Substance Name | DEXAMETHASONE SODIUM PHOSPHATE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
