Ketoprofen
- Product NDC
- 68788-9088
- 11-digit product format
- 687889088
- Labeler code
- 68788
- Product ID
- 68788-9088_4a7b1bed-5969-47a3-9103-5c6b7101d7a1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ketoprofen
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA073517
- Marketing category
- ANDA
- Marketing start
- 2011-01-18
- Marketing end
- 0000-00-00
- Substance
- KETOPROFEN
- Active strength
- 75 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