Ibuprofen
- Product NDC
- 61715-168
- 11-digit product format
- 617150168
- Labeler code
- 61715
- Product ID
- 61715-168_401191fe-7ed4-468c-98cc-e00f2c0bcc64
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Kinray, Inc.
- Application
- ANDA091237
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 61715-168-50 | 2025-05-20 | C162847 | 48780-1 | 9d75b9d1-0ec1-f424-e053-dadaa90a57ce | 7cc53a7b-dff7-487a-b0e2-eef7f69b83ef |
| 61715-168-51 | 2025-05-20 | C162847 | 48780-1 | 9d75b9d1-0ec1-f424-e053-dadaa90a57ce | 7cc53a7b-dff7-487a-b0e2-eef7f69b83ef |
| 61715-168-50 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-0ec1-f424-e053-dadaa90a57ce | 7cc53a7b-dff7-487a-b0e2-eef7f69b83ef |
| 61715-168-51 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-0ec1-f424-e053-dadaa90a57ce | 7cc53a7b-dff7-487a-b0e2-eef7f69b83ef |