Ibuprofen
- Product NDC
- 68998-111
- 11-digit product format
- 689980111
- Labeler code
- 68998
- Product ID
- 68998-111_bed62b69-93f0-3b72-e053-2a95a90abc26
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Marc Glassman, Inc.
- Application
- ANDA091355
- Marketing category
- ANDA
- Marketing start
- 2009-06-01
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68998-111-03 | 68998011103 | 1 BOTTLE, PLASTIC in 1 CARTON (68998-111-03) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC | 2009-06-01 | 0000-00-00 | No | No | Current |