Ketoprofen
- Product NDC
- 21695-340
- 11-digit product format
- 216950340
- Labeler code
- 21695
- Product ID
- 21695-340_9bc31f67-cfce-4ad6-9c07-3845ead3542c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ketoprofen
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA074035
- Marketing category
- ANDA
- Marketing start
- 2010-04-20
- Marketing end
- 0000-00-00
- Substance
- KETOPROFEN
- Active strength
- 50 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 |
|---|
| 21695-340-72 | Ketoprofen | 120 in 1 BOTTLE | CAPSULE | 120 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-340 | KETOPROFEN CAPSULE [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 1 package rows | 20110104_9bc31f67-cfce-4ad6-9c07-3845ead3542c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-340-72 | 21695034072 | 120 in 1 BOTTLE | Historical |