dry eye test

Generic: fluorescein sodium

Labeler: nomax inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name dry eye test
Generic Name fluorescein sodium
Labeler nomax inc.
Dosage Form STRIP
Routes
OPHTHALMIC
Active Ingredients

fluorescein sodium .12 mg/1

Manufacturer
Nomax Inc.

Identifiers & Regulatory

Product NDC 51801-008
Product ID 51801-008_7490418c-b489-4b90-bc3d-33ed71231e2d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2013-12-05

Pharmacologic Class

Classes
diagnostic dye [epc] dyes [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51801008
Hyphenated Format 51801-008

Supplemental Identifiers

UNII
93X55PE38X

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name dry eye test (source: ndc)
Generic Name fluorescein sodium (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • .12 mg/1
source: ndc
Packaging
  • 50 POUCH in 1 CARTON (51801-008-15) / 2 STRIP in 1 POUCH
source: ndc

Packages (1)

51801-008-15 50 POUCH in 1 CARTON (51801-008-15) / 2 STRIP in 1 POUCH

Ingredients (1)

fluorescein sodium (.12 mg/1)

Linked Drug Pages (1)

Dry Eye Test ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "7490418c-b489-4b90-bc3d-33ed71231e2d", "openfda": {"unii": ["93X55PE38X"], "spl_set_id": ["04866053-f973-471e-b3bc-241fb76303a2"], "manufacturer_name": ["Nomax Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 POUCH in 1 CARTON (51801-008-15)  / 2 STRIP in 1 POUCH", "package_ndc": "51801-008-15", "marketing_start_date": "20131205"}], "brand_name": "Dry Eye Test", "product_id": "51801-008_7490418c-b489-4b90-bc3d-33ed71231e2d", "dosage_form": "STRIP", "pharm_class": ["Diagnostic Dye [EPC]", "Dyes [MoA]"], "product_ndc": "51801-008", "generic_name": "Fluorescein Sodium", "labeler_name": "Nomax Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dry Eye Test", "active_ingredients": [{"name": "FLUORESCEIN SODIUM", "strength": ".12 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20131205", "listing_expiration_date": "20261231"}