Ibuprofen
- Product NDC
- 21130-292
- 11-digit product format
- 211300292
- Labeler code
- 21130
- Product ID
- 21130-292_305196c7-1d56-4a02-8770-54015b2d1b76
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Better Living Brands, LLC
- Application
- ANDA075010
- Marketing category
- ANDA
- Marketing start
- 1988-05-24
- Marketing end
- 2019-09-12
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record