equaline ibuprofen pm
- Product NDC
- 41163-561
- 11-digit product format
- 411630561
- Labeler code
- 41163
- Product ID
- 41163-561_5b5234a6-8340-44d2-af6d-ef8307d46671
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine citrate, Ibuprofen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Supervalu Inc
- Application
- ANDA079113
- Marketing category
- ANDA
- Marketing start
- 2012-01-11
- 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