smart sense ibuprofen
- Product NDC
- 49738-517
- 11-digit product format
- 497380517
- Labeler code
- 49738
- Product ID
- 49738-517_24804570-5212-4c9d-a4ed-9bc818114646
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Kmart Corporation
- Application
- ANDA077349
- Marketing category
- ANDA
- Marketing start
- 2010-06-18
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record