Flurbiprofen Sodium
- Product NDC
- 50090-0625
- 11-digit product format
- 500900625
- Labeler code
- 50090
- Product ID
- 50090-0625_f32d7200-089a-4e51-9142-0cde2e1b2144
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Flurbiprofen Sodium
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- A-S Medication Solutions
- Application
- ANDA074447
- Marketing category
- ANDA
- Marketing start
- 1995-01-04
- Marketing end
- 0000-00-00
- Substance
- FLURBIPROFEN SODIUM
- Active strength
- 0 mg/mL
- 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