Ibuprofen
- Product NDC
- 59726-186
- 11-digit product format
- 597260186
- Labeler code
- 59726
- Product ID
- 59726-186_8178201d-74a1-487a-9ac6-6449948d943a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA076460
- Marketing category
- ANDA
- Marketing start
- 2015-11-30
- Marketing end
- 2020-12-31
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record