ibuprofen
- Product NDC
- 69842-709
- 11-digit product format
- 698420709
- Labeler code
- 69842
- Product ID
- 69842-709_19adf0e9-5e97-4cc7-b637-e7e46d26d526
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- CVS Pharmacy
- Application
- ANDA206581
- Marketing category
- ANDA
- Marketing start
- 2018-02-02
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN SODIUM
- Active strength
- 256 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record