ibuprofen pm
- Product NDC
- 59779-413
- 11-digit product format
- 597790413
- Labeler code
- 59779
- Product ID
- 59779-413_885ee5e1-acc1-4b3d-9628-4d1d82c1ca33
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine citrate, Ibuprofen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- CVS Pharmacy
- Application
- ANDA079113
- Marketing category
- ANDA
- Marketing start
- 2010-03-02
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE CITRATE; IBUPROFEN
- Active strength
- 38 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record