RESCRIPTOR

Product NDC
49702-225
11-digit product format
497020225
Labeler code
49702
Product ID
49702-225_48868879-0671-42c2-ab7b-09ec8b98dcbe
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
delavirdine mesylate
Dosage form
TABLET
Route
ORAL
Labeler
ViiV Healthcare Company
Application
NDA020705
Marketing category
NDA
Marketing start
2012-04-11
Marketing end
2020-08-31
Substance
DELAVIRDINE MESYLATE
Active strength
200 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
49702-225-17EA - Each49702-225050cdfe8-4bd6-4b8b-91fd-b422ecf91b6b12013-02-13