Ibuprofen
- Product NDC
- 41250-221
- 11-digit product format
- 412500221
- Labeler code
- 41250
- Product ID
- 41250-221_64bb61ee-2065-4e59-b4e3-d8e436436745
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- MEIJER, INC.
- Application
- ANDA202300
- Marketing category
- ANDA
- Marketing start
- 2018-03-31
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41250-221-16 | 41250022116 | 2 BOTTLE, PLASTIC in 1 BOX (41250-221-16) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2018-03-31 | 0000-00-00 | No | No | Current |
| 41250-221-30 | 41250022130 | 300 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (41250-221-30) | 2018-03-31 | 0000-00-00 | No | No | Current |
| 41250-221-40 | 41250022140 | 1 BOTTLE, PLASTIC in 1 BOX (41250-221-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2018-03-31 | 0000-00-00 | No | No | Current |
| 41250-221-80 | 41250022180 | 1 BOTTLE, PLASTIC in 1 BOX (41250-221-80) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2018-03-31 | 0000-00-00 | No | No | Current |