Ketoprofen
- Product NDC
- 69336-127
- 11-digit product format
- 693360127
- Labeler code
- 69336
- Product ID
- 69336-127_24cb9c03-a57b-4329-9d90-239fbd54a84d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ketoprofen
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Sterling-Knight Pharmaceuticals LLC
- Application
- ANDA074014
- Marketing category
- ANDA
- Marketing start
- 2019-06-19
- Marketing end
- 0000-00-00
- Substance
- KETOPROFEN
- Active strength
- 25 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69336-127-10 | 69336012710 | 100 CAPSULE in 1 BOTTLE (69336-127-10) | 100 capsule | 2019-06-19 | 0000-00-00 | No | No | Current |
| 69336-127-11 | 69336012711 | 1000 CAPSULE in 1 BOTTLE (69336-127-11) | 1000 capsule | 2019-06-19 | 0000-00-00 | No | No | Current |