Ibuprofen
- Product NDC
- 59726-022
- 11-digit product format
- 597260022
- Labeler code
- 59726
- Product ID
- 59726-022_e61ce148-a7ad-48ba-a77f-3be65a0dc3f3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA078682
- Marketing category
- ANDA
- Marketing start
- 2014-07-31
- Marketing end
- 2019-12-31
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record