ketoprofen
- Product NDC
- 23155-020
- 11-digit product format
- 231550020
- Labeler code
- 23155
- Product ID
- 23155-020_a208a105-83b3-4b1a-b552-9884cf2cb891
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ketoprofen
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Application
- ANDA074014
- Marketing category
- ANDA
- Marketing start
- 2018-06-14
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 23155-020-01 | 23155002001 | 100 CAPSULE in 1 BOTTLE (23155-020-01) | 100 capsule | 2018-06-14 | 0000-00-00 | No | No | Current |
| 23155-020-05 | 23155002005 | 500 CAPSULE in 1 BOTTLE (23155-020-05) | 500 capsule | 2018-06-14 | 0000-00-00 | No | No | Current |