ibuprofen pm
- Product NDC
- 41250-413
- 11-digit product format
- 412500413
- Labeler code
- 41250
- Product ID
- 41250-413_35cf786a-8ee6-4bdf-8418-7c2d2f5c2f2d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine citrate, Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- ANDA079113
- Marketing category
- ANDA
- Marketing start
- 2015-04-23
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41250-413-27 | 41250041327 | 1 BOTTLE in 1 CARTON (41250-413-27) > 80 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2015-04-23 | 0000-00-00 | No | No | Current |