NDC 51801-008

Dry Eye Test

Fluorescein Sodium

Dry Eye Test is a Ophthalmic Strip in the Human Prescription Drug category. It is labeled and distributed by Nomax Inc.. The primary component is Fluorescein Sodium.

Product ID51801-008_08dd04c1-ca76-4b5d-ae29-1479238743b2
NDC51801-008
Product TypeHuman Prescription Drug
Proprietary NameDry Eye Test
Generic NameFluorescein Sodium
Dosage FormStrip
Route of AdministrationOPHTHALMIC
Marketing Start Date2013-12-05
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameNomax Inc.
Substance NameFLUORESCEIN SODIUM
Active Ingredient Strength0 mg/1
Pharm ClassesDiagnostic Dye [EPC],Dyes [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 51801-008-15

50 POUCH in 1 CARTON (51801-008-15) > 2 STRIP in 1 POUCH
Marketing Start Date2013-12-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51801-008-15 [51801000815]

Dry Eye Test STRIP
Marketing CategoryUNAPPROVED DRUG OTHER
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-12-05

Drug Details

Active Ingredients

IngredientStrength
FLUORESCEIN SODIUM.12 mg/1

OpenFDA Data

SPL SET ID:04866053-f973-471e-b3bc-241fb76303a2
Manufacturer
UNII

Pharmacological Class

  • Diagnostic Dye [EPC]
  • Dyes [MoA]

NDC Crossover Matching brand name "Dry Eye Test" or generic name "Fluorescein Sodium"

NDCBrand NameGeneric Name
51801-008Dry Eye TestFluorescein Sodium
17478-250AK-FLUORfluorescein sodium
17478-253AK-FLUORfluorescein sodium
50090-4535AK-FLUORfluorescein sodium
17238-900BioGloFluorescein Sodium
0065-0092FLUORESCITEfluorescein sodium
17478-403FUL-GLOFluorescein Sodium
17478-404FUL-GLOFluorescein Sodium
51801-003GloStripsFluorescein Sodium
51801-009GloStripsFluorescein Sodium

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