Ibuprofen
- Product NDC
- 71335-0223
- 11-digit product format
- 713350223
- Labeler code
- 71335
- Product ID
- 71335-0223_dab37f4f-1040-4df2-aaf8-502f63240229
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA091239
- Marketing category
- ANDA
- Marketing start
- 2016-03-01
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 71335-0223-0 | 71335022300 | 90 TABLET in 1 BOTTLE (71335-0223-0) | 90 tablet | 2016-04-29 | 0000-00-00 | No | No | Current |
| 71335-0223-1 | 71335022301 | 20 TABLET in 1 BOTTLE (71335-0223-1) | 20 tablet | 2016-04-29 | 0000-00-00 | No | No | Current |
| 71335-0223-2 | 71335022302 | 15 TABLET in 1 BOTTLE (71335-0223-2) | 15 tablet | 2016-04-29 | 0000-00-00 | No | No | Current |
| 71335-0223-3 | 71335022303 | 30 TABLET in 1 BOTTLE (71335-0223-3) | 30 tablet | 2016-04-29 | 0000-00-00 | No | No | Current |
| 71335-0223-4 | 71335022304 | 100 TABLET in 1 BOTTLE (71335-0223-4) | 100 tablet | 2016-04-29 | 0000-00-00 | No | No | Current |
| 71335-0223-5 | 71335022305 | 60 TABLET in 1 BOTTLE (71335-0223-5) | 60 tablet | 2016-04-29 | 0000-00-00 | No | No | Current |
| 71335-0223-6 | 71335022306 | 50 TABLET in 1 BOTTLE (71335-0223-6) | 50 tablet | 2016-04-29 | 0000-00-00 | No | No | Current |
| 71335-0223-7 | 71335022307 | 40 TABLET in 1 BOTTLE (71335-0223-7) | 40 tablet | 2016-04-29 | 0000-00-00 | No | No | Current |
| 71335-0223-8 | 71335022308 | 10 TABLET in 1 BOTTLE (71335-0223-8) | 10 tablet | 2016-04-29 | 0000-00-00 | No | No | Current |
| 71335-0223-9 | 71335022309 | 56 TABLET in 1 BOTTLE (71335-0223-9) | 56 tablet | 2016-04-29 | 0000-00-00 | No | No | Current |