Ketoprofen
- Product NDC
- 0682-0150
- 11-digit product format
- 006820150
- Labeler code
- 0682
- Product ID
- 0682-0150_4e7bceb6-dcb6-c5e0-e063-6294a90a101e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ketoprofen
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Marnel Pharmaceuticals, Inc.
- Application
- ANDA074014
- Marketing category
- ANDA
- Marketing start
- 2026-04-02
- Substance
- KETOPROFEN
- Active strength
- 75 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ketoprofen
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| KETOPROFEN | 75 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 90Y4QC304K |
| Rxcui | 197856 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0682-0150-60 | Ketoprofen | 60 in 1 BOTTLE | CAPSULE | 60 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0682-0150-60 | 00682015060 | 60 CAPSULE in 1 BOTTLE (0682-0150-60) | 60 capsule | 2026-04-02 | No | No | Current |