Ibuprofen and Diphenhydramine HCl
- Product NDC
- 49035-065
- 11-digit product format
- 490350065
- Labeler code
- 49035
- Product ID
- 49035-065_1b5dbbc9-023b-481e-be91-954e7e375cb5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN, DIPHENHYDRAMINE HCL
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- EQUATE (Wal-Mart Stores, Inc.)
- Application
- ANDA090397
- Marketing category
- ANDA
- Marketing start
- 2015-12-31
- Marketing end
- 2024-04-26
- Substance
- IBUPROFEN; DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 200 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49035-065-40 | 49035006540 | 1 BOTTLE, PLASTIC in 1 BOX (49035-065-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2015-12-31 | 2024-04-26 | No | No | Current |