Ibuprofen PM
- Product NDC
- 37012-050
- 11-digit product format
- 370120050
- Labeler code
- 37012
- Product ID
- 37012-050_74a9502d-0850-41ab-abd8-a1de90b82dbf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- diphenhydramine citrate, ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Shopko Stores Operating Co., LLC
- Application
- ANDA079113
- Marketing category
- ANDA
- Marketing start
- 2016-08-03
- 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 |
|---|
| 37012-050-27 | 37012005027 | 1 BOTTLE in 1 CARTON (37012-050-27) > 80 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2016-08-03 | 0000-00-00 | No | No | Current |