berkley and jensen ibuprofen pm
- Product NDC
- 68391-050
- 11-digit product format
- 683910050
- Labeler code
- 68391
- Product ID
- 68391-050_c3381086-84a1-4fb7-b601-5443fa435798
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- diphenhydramine citrate, ibuprofen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- BJWC
- Application
- ANDA079113
- Marketing category
- ANDA
- Marketing start
- 2009-04-27
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68391-050-48 | 68391005048 | 1 BOTTLE in 1 CARTON (68391-050-48) > 180 TABLET, COATED in 1 BOTTLE | 1 bottle | 2009-04-27 | 0000-00-00 | No | No | Current |
| 68391-050-82 | 68391005082 | 200 TABLET, COATED in 1 BOTTLE (68391-050-82) | | 2017-01-18 | 0000-00-00 | No | No | Current |