NDC 16030-302 - Aurovisc Lubricant HYPROMELLOSE 2208 (15000 MPA.S) Solution/Drops

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
16030-302
Package NDCs from labels
16030-302-02
Manufacturer
Aurolab
Effective date
2023-01-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Aurovisc Lubricant HYPROMELLOSE 2208 (15000 MPA.S) Solution/Drops - AurolabAurolab2023-01-11HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
16030-302-022025-01-30C16284748780-12cef2736-6f66-d83d-e063-dadaa90ab31ff27a44dc-c420-ed92-e053-2995a90a1640

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
16030-302-02Aurovisc Lubricant HYPROMELLOSE 2208 (15000 MPA.S) Solution/Drops2 mL in 1 SYRINGE, GLASSSOLUTION/ DROPS21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
16030-302AUROVISC LUBRICANT HYPROMELLOSE 2208 (15000 MPA.S) SOLUTION/DROPS (HYPROMELLOSE OPHTHALMIC SOLUTION 2% W/V) SOLUTION/ DROPS [AUROLAB]11 package rows20230118_f27a44dc-c420-ed92-e053-2995a90a1640.zip