Ketoprofen
- Product NDC
- 67296-0369
- 11-digit product format
- 672960369
- Labeler code
- 67296
- Product ID
- 67296-0369_1cc23bf2-170e-4170-9299-bfaa55d06ec7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ketoprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug Inc.
- Application
- ANDA073517
- Marketing category
- ANDA
- Marketing start
- 2011-01-18
- Marketing end
- 0000-00-00
- Substance
- KETOPROFEN
- Active strength
- 75 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 67296-0369-2 | Ketoprofen | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0369 | KETOPROFEN TABLET [REDPHARM DRUG INC.] | 1 | Legacy NDC, 1 package rows | 20110727_e5eb6170-20a3-4d21-a8ee-7483b521a286.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67296-0369-2 | 67296036902 | 30 in 1 BOTTLE | Historical |