Ibuprofen
- Product NDC
- 61715-059
- 11-digit product format
- 617150059
- Labeler code
- 61715
- Product ID
- 61715-059_24471a0d-6862-475c-9586-e78b4c6897f9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Kinray
- Application
- ANDA091239
- Marketing category
- ANDA
- Marketing start
- 2011-07-25
- 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#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61715-059 | IBUPROFEN (IBUPROFEN) TABLET [KINRAY] | 2 | Legacy NDC | 20130531_d01782d0-5019-48a2-af66-0f0c03cf95e2.zip |