Ulesfia

Product NDC
23594-780
11-digit product format
235940780
Labeler code
23594
Product ID
23594-780_3f0364fa-e779-4522-84ca-a5229ee3ca52
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
benzyl alcohol
Dosage form
LOTION
Route
TOPICAL
Labeler
Cerecor, Inc.
Application
NDA022129
Marketing category
NDA
Marketing start
2014-07-16
Marketing end
0000-00-00
Substance
BENZYL ALCOHOL
Active strength
50 mg/g
Pharmacologic classes
Pediculicide [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
23594-780-88GM - Gram23594-78082afcba9-b701-4a39-9886-1a8f94d3fa7312014-08-01