RESCRIPTOR

Product NDC
49702-209
11-digit product format
497020209
Labeler code
49702
Product ID
49702-209_76364ac0-3a4e-41d2-8406-6a5c1c94e6cf
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
delavirdine mesylate
Dosage form
TABLET
Route
ORAL
Labeler
ViiV Healthcare Company
Application
NDA020705
Marketing category
NDA
Marketing start
2010-10-13
Marketing end
2019-05-31
Substance
DELAVIRDINE MESYLATE
Active strength
100 mg/1
Pharmacologic classes
Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA],Non-Nucleoside Analog [EXT]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49702-209-24EA - Each49702-20967277814-9759-4bc6-b54b-0b0e4203385212012-07-24