Flurbiprofen
- Product NDC
- 50090-0509
- 11-digit product format
- 500900509
- Labeler code
- 50090
- Product ID
- 50090-0509_07407986-40e8-4fbf-b15b-5be4f3ec7e15
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Flurbiprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074431
- Marketing category
- ANDA
- Marketing start
- 1995-06-02
- Marketing end
- 0000-00-00
- Substance
- FLURBIPROFEN
- Active strength
- 100 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record