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FLUCAINE
FLUCAINE - 54799-507-21 - (Fluorescein Sodium and Proparacaine Hydrochloride)
Drug Information of FLUCAINE
| Product NDC: | 54799-507 |
| Proprietary Name: | FLUCAINE |
| Non Proprietary Name: | Fluorescein Sodium and Proparacaine Hydrochloride |
| Active Ingredient(s): | 2.5; 5 mg/mL; mg/mL & nbsp; Fluorescein Sodium and Proparacaine Hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FLUCAINE
| Product NDC: | 54799-507 |
| Labeler Name: | OCuSOFT, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19890330 |
Package Information of FLUCAINE
| Package NDC: | 54799-507-21 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (54799-507-21) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of FLUCAINE
| NDC Code | 54799-507-21 |
| Proprietary Name | FLUCAINE |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (54799-507-21) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 54799-507 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluorescein Sodium and Proparacaine Hydrochloride |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19890330 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | OCuSOFT, Inc. |
| Substance Name | FLUORESCEIN SODIUM; PROPARACAINE HYDROCHLORIDE |
| Strength Number | 2.5; 5 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Diagnostic Dye [EPC],Dyes [MoA],Local Anesthesia [PE],Local Anesthetic [EPC] |
