Ibuprofen
- Product NDC
- 53002-5710
- 11-digit product format
- 530025710
- Labeler code
- 53002
- Product ID
- 53002-5710_99d103ff-dd51-4a7b-8d32-b5d3bafed7f4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-5710-0 | 53002571000 | 100 TABLET in 1 BOTTLE (53002-5710-0) | 100 tablet | 2018-10-01 | 0000-00-00 | No | No | Current |
| 53002-5710-3 | 53002571003 | 30 TABLET in 1 BOTTLE (53002-5710-3) | 30 tablet | 2018-10-01 | 0000-00-00 | No | No | Current |
| 53002-5710-5 | 53002571005 | 50 TABLET in 1 BOTTLE (53002-5710-5) | 50 tablet | 2018-10-01 | 0000-00-00 | No | No | Current |