Ketoprofen
- Product NDC
- 68788-6400
- 11-digit product format
- 687886400
- Labeler code
- 68788
- Product ID
- 68788-6400_7da9a88a-6dd4-4c85-b613-53924c2f8977
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ketoprofen
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA073516
- Marketing category
- ANDA
- Marketing start
- 2016-05-31
- Marketing end
- 0000-00-00
- Substance
- KETOPROFEN
- Active strength
- 50 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