Ibuprofen
- Product NDC
- 68071-3074
- 11-digit product format
- 680713074
- Labeler code
- 68071
- Product ID
- 68071-3074_a4febf51-bfe6-1902-e053-2a95a90ab778
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA091239
- Marketing category
- ANDA
- Marketing start
- 2016-03-01
- Marketing end
- 2020-12-31
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record