Ibuprofen
- Product NDC
- 59726-235
- 11-digit product format
- 597260235
- Labeler code
- 59726
- Product ID
- 59726-235_8d09357f-779f-4ac2-9332-91a6ed918ee2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA076460
- Marketing category
- ANDA
- Marketing start
- 2014-11-30
- Marketing end
- 2021-12-30
- Substance
- IBUPROFEN
- Active strength
- 200 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 |
|---|
| 59726-235-24 | 59726023524 | 1 BOTTLE, PLASTIC in 1 BOX (59726-235-24) > 24 TABLET, COATED in 1 BOTTLE, PLASTIC | 2014-11-30 | 2021-12-30 | No | No | Current |
| 59726-235-40 | 59726023540 | 1 BOTTLE, PLASTIC in 1 BOX (59726-235-40) > 40 TABLET, COATED in 1 BOTTLE, PLASTIC | 2014-11-30 | 2021-12-30 | No | No | Current |