Ibuprofen PM
- Product NDC
- 11673-265
- 11-digit product format
- 116730265
- Labeler code
- 11673
- Product ID
- 11673-265_e879a9cd-e204-4ce6-8a33-73c85fc3c249
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN, DIPHENHYDRAMINE HCL
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- TARGET Corporation
- Application
- ANDA090397
- Marketing category
- ANDA
- Marketing start
- 2018-01-31
- Marketing end
- 2022-12-30
- 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 |
|---|
| 11673-265-40 | 11673026540 | 1 BOTTLE, PLASTIC in 1 BOX (11673-265-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2018-01-31 | 2022-12-30 | No | No | Current |