BEVYXXA
- Product NDC
- 69853-0202
- 11-digit product format
- 698530202
- Labeler code
- 69853
- Product ID
- 69853-0202_2e844c6c-8a74-441c-bb92-30c34b0dce08
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- betrixaban
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- Portola Pharmaceuticals, Inc.
- Application
- NDA208383
- Marketing category
- NDA
- Marketing start
- 2017-07-07
- Marketing end
- 0000-00-00
- Substance
- BETRIXABAN
- Active strength
- 40 mg/1
- Pharmacologic classes
- Factor Xa Inhibitors [MoA],Factor Xa Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record