smart sense ibuprofen pm
- Product NDC
- 49738-191
- 11-digit product format
- 497380191
- Labeler code
- 49738
- Product ID
- 49738-191_4c75b431-adad-452a-94c5-cdae73ed4966
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- diphenhydramine citrate, ibuprofen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Kmart Corporation
- Application
- ANDA079113
- Marketing category
- ANDA
- Marketing start
- 2010-05-27
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE CITRATE; IBUPROFEN
- Active strength
- 38 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record