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NDC 00065-0092-65 FLUORESCITE 100 mg/mL Details
FLUORESCITE 100 mg/mL
FLUORESCITE is a OPHTHALMIC INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Alcon, Inc.. The primary component is FLUORESCEIN SODIUM.
Product Information
NDC | 00065-0092 |
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Product ID | 0065-0092_85861756-9727-4a43-8a4e-48564e341c48 |
Associated GPIs | 86806010202010 |
GCN Sequence Number | 006830 |
GCN Sequence Number Description | fluorescein sodium VIAL 500 MG/5ML INTRAVEN |
HIC3 | Q2U |
HIC3 Description | EYE DIAGNOSTIC AGENTS |
GCN | 27760 |
HICL Sequence Number | 002908 |
HICL Sequence Number Description | FLUORESCEIN SODIUM |
Brand/Generic | Brand |
Proprietary Name | FLUORESCITE |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | fluorescein sodium |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | INJECTION, SOLUTION |
Route | OPHTHALMIC |
Active Ingredient Strength | 100 |
Active Ingredient Units | mg/mL |
Substance Name | FLUORESCEIN SODIUM |
Labeler Name | Alcon, Inc. |
Pharmaceutical Class | Diagnostic Dye [EPC], Dyes [MoA] |
DEA Schedule | n/a |
Marketing Category | NDA |
Application Number | NDA021980 |
Listing Certified Through | 2024-12-31 |
Package
NDC 00065-0092-65 (00065009265)
NDC Package Code | 0065-0092-65 |
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Billing NDC | 00065009265 |
Package | 12 VIAL in 1 CARTON (0065-0092-65) / 5 mL in 1 VIAL |
Marketing Start Date | 1972-09-15 |
NDC Exclude Flag | N |
Pricing Information | N/A |