Dry Eye Test
Dry Eye Test
Approved
Approval ID
04866053-f973-471e-b3bc-241fb76303a2
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 23, 2019
Manufacturers
FDA
Nomax Inc.
DUNS: 103220273
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Fluorescein Sodium
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51801-008
Product Classification
G
Generic Name
Fluorescein Sodium
Product Specifications
Route of AdministrationOPHTHALMIC
Effective DateDecember 23, 2019
FDA Product Classification
INGREDIENTS (1)
Fluorescein SodiumActive
Quantity: 0.12 mg in 1 1
Code: 93X55PE38X
Classification: ACTIM