diflunisal
- Product NDC
- 23155-673
- 11-digit product format
- 231550673
- Labeler code
- 23155
- Product ID
- 23155-673_55c94869-230d-4e43-b4a1-bc723334342e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diflunisal
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc.
- Application
- ANDA202845
- Marketing category
- ANDA
- Marketing start
- 2012-03-08
- Marketing end
- 0000-00-00
- Substance
- DIFLUNISAL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record