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FLUORESCITE
FLUORESCITE - 0065-0092-05 - (fluorescein sodium)
Drug Information of FLUORESCITE
| Product NDC: | 0065-0092 |
| Proprietary Name: | FLUORESCITE |
| Non Proprietary Name: | fluorescein sodium |
| Active Ingredient(s): | 100 mg/mL & nbsp; fluorescein sodium |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FLUORESCITE
| Product NDC: | 0065-0092 |
| Labeler Name: | Alcon, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021980 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19720915 |
Package Information of FLUORESCITE
| Package NDC: | 0065-0092-05 |
| Package Description: | 5 mL in 1 VIAL (0065-0092-05) |
NDC Information of FLUORESCITE
| NDC Code | 0065-0092-05 |
| Proprietary Name | FLUORESCITE |
| Package Description | 5 mL in 1 VIAL (0065-0092-05) |
| Product NDC | 0065-0092 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluorescein sodium |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19720915 |
| Marketing Category Name | NDA |
| Labeler Name | Alcon, Inc. |
| Substance Name | FLUORESCEIN SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Diagnostic Dye [EPC],Dyes [MoA] |
