MedPath

GloStrips

GloStrips 1.0

Approved
Approval ID

d06a4432-c76c-4e2a-abec-6bc5b4e82d51

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 Code51801-009
Product Classification
G
Generic Name
Fluorescein Sodium
Product Specifications
Route of AdministrationOPHTHALMIC
Effective DateDecember 23, 2019
FDA Product Classification

INGREDIENTS (1)

Fluorescein SodiumActive
Quantity: 1 mg in 1 1
Code: 93X55PE38X
Classification: ACTIM

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GloStrips - FDA Drug Approval Details