FENOPROFEN CALCIUM
- Product NDC
- 54288-132
- 11-digit product format
- 542880132
- Labeler code
- 54288
- Product ID
- 54288-132_a03faba1-e4b5-4c21-988a-64dbcf0d6a61
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENOPROFEN CALCIUM
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- BPI Labs LLC
- Application
- NDA017604
- Marketing category
- NDA
- Marketing start
- 2016-07-06
- Marketing end
- 0000-00-00
- Substance
- FENOPROFEN CALCIUM
- Active strength
- 400 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
FDA-Initiated Inactive NDC Indexing#