Ibuprofen
- Product NDC
- 33992-0291
- 11-digit product format
- 339920291
- Labeler code
- 33992
- Product ID
- 33992-0291_f3f9a6be-5adc-4289-9b7e-091cb758bbb2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- GREENBRIER INTERNATIONAL, INC.
- Application
- ANDA075010
- Marketing category
- ANDA
- Marketing start
- 1988-05-24
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 33992-0291-0 | 33992029100 | 1 BOTTLE, PLASTIC in 1 CARTON (33992-0291-0) > 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 1988-05-24 | 0000-00-00 | No | No | Current |
| 33992-0291-2 | 33992029102 | 1 BOTTLE, PLASTIC in 1 CARTON (33992-0291-2) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 1988-05-24 | 0000-00-00 | No | No | Current |
| 33992-0291-5 | 33992029105 | 1 BOTTLE, PLASTIC in 1 CARTON (33992-0291-5) > 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 1988-05-24 | 0000-00-00 | No | No | Current |