Ketoprofen
- Product NDC
- 66267-126
- 11-digit product format
- 662670126
- Labeler code
- 66267
- Product ID
- 66267-126_9cbdfd9b-927b-533e-e053-2995a90a6fd9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ketoprofen
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA073517
- Marketing category
- ANDA
- Marketing start
- 1993-01-01
- Marketing end
- 0000-00-00
- Substance
- KETOPROFEN
- Active strength
- 75 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record