FINACEA FOAM

Product NDC
50419-829
11-digit product format
504190829
Labeler code
50419
Product ID
50419-829_b23e5be7-91a5-4981-839c-655615884b21
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
azelaic acid
Dosage form
AEROSOL, FOAM
Route
TOPICAL
Labeler
Bayer HealthCare Pharmaceuticals Inc.
Application
NDA207071
Marketing category
NDA
Marketing start
2015-08-03
Marketing end
0000-00-00
Substance
AZELAIC ACID
Active strength
0 g/g
Pharmacologic classes
Decreased Protein Synthesis [PE],Decreased Sebaceous Gland Activity [PE]
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
50419-829-01GM - Gram50419-82966d6ff59-5cd4-4d01-b8ff-74f1b222b2c412015-09-10