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