ketoprofen
- Product NDC
- 23155-021
- 11-digit product format
- 231550021
- Labeler code
- 23155
- Product ID
- 23155-021_d298ce92-b8cb-4bd0-a71e-ff5378f2af14
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ketoprofen
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.
- Application
- ANDA074014
- Marketing category
- ANDA
- Marketing start
- 2020-01-28
- Marketing end
- 2022-01-31
- Substance
- KETOPROFEN
- Active strength
- 50 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 23155-021-01 | 23155002101 | 100 CAPSULE in 1 BOTTLE (23155-021-01) | 100 capsule | 2020-01-28 | 0000-00-00 | No | No | Current |
| 23155-021-05 | 23155002105 | 500 CAPSULE in 1 BOTTLE (23155-021-05) | 500 capsule | 2020-01-28 | 0000-00-00 | No | No | Current |