Ketoprofen
- Product NDC
- 50090-2729
- 11-digit product format
- 500902729
- Labeler code
- 50090
- Product ID
- 50090-2729_65a4088c-d89a-4b2e-ad45-762b8691485f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ketoprofen
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA073516
- Marketing category
- ANDA
- Marketing start
- 1993-01-01
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2729-0 | Ketoprofen | 45 in 1 BOTTLE | CAPSULE | 45 | | 14 |
| 50090-2729-1 | Ketoprofen | 20 in 1 BOTTLE | CAPSULE | 20 | | 14 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2729 | KETOPROFEN CAPSULE [A-S MEDICATION SOLUTIONS] | 14 | Legacy NDC, 2 package rows | 20171012_43efd625-4983-47b1-9532-5b63eea93a4e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2729-0 | 50090272900 | 45 in 1 BOTTLE | Historical |
| 50090-2729-1 | 50090272901 | 20 in 1 BOTTLE | Historical |