Flurbiprofen
- Product NDC
- 49999-311
- 11-digit product format
- 499990311
- Labeler code
- 49999
- Product ID
- 49999-311_769ab3f2-fe6b-4896-b2f2-18ac79a85ed6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Flurbiprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
- Application
- ANDA074431
- Marketing category
- ANDA
- Marketing start
- 2012-03-07
- Marketing end
- 0000-00-00
- Substance
- FLURBIPROFEN
- Active strength
- 100 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record