POTIGA
- Product NDC
- 0173-0810
- 11-digit product format
- 001730810
- Labeler code
- 0173
- Product ID
- 0173-0810_38028c77-169f-47e4-9d61-5f625f3627f3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ezogabine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- GlaxoSmithKline LLC
- Application
- NDA022345
- Marketing category
- NDA
- Marketing start
- 2012-04-19
- Marketing end
- 2019-07-31
- Substance
- EZOGABINE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Potassium Channel Openers [MoA],Potassium Channel Opener [EPC]
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record