Ibuprofen PM
- Product NDC
- 50844-611
- 11-digit product format
- 508440611
- Labeler code
- 50844
- Product ID
- 50844-611_005e4a1a-aab3-4a10-a467-d9296dd5bd9f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine hydrochloride, ibuprofen
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- L.N.K. International, Inc.
- Application
- ANDA200888
- Marketing category
- ANDA
- Marketing start
- 2013-07-08
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN
- Active strength
- 25 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50844-611-19 | 50844061119 | 1 BLISTER PACK in 1 CARTON (50844-611-19) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK | 1 blister pack | 2013-07-08 | 0000-00-00 | No | No | Current |