Home NDC 0095-0073 HYLASE Wound
Product NDC 0095-0073
11-digit product format 000950073
Labeler code 0095
Product ID 0095-0073_49a31634-a2f7-46fa-ba93-fb2e5d99c0e4
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Sodium Hyaluronate
Dosage form GEL
Route TOPICAL
Labeler ECR Pharmaceuticals Co., Inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2012-01-06
Marketing end 0000-00-00
Substance HYALURONATE SODIUM
Active strength 3 g/100g
NDC exclude flag E
Listing certified through 2017-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 0095-0073-75 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 0095-0073-75 110d247fa046…a55b01930146…
FDA-Initiated Inactive NDC Indexing#