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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0095-0073-752019-11-13C16284748780-197449f38-ceb1-f6ea-e053-dbdaa90aa7037d221721-f86e-457f-834d-c12c5e7210fc

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0095-0073-75GM - Gram0095-007386cc7fd5-9ec5-4ea1-b86a-8e951f7d6afb12013-02-13