IBUPROFEN
- Product NDC
- 55315-940
- 11-digit product format
- 553150940
- Labeler code
- 55315
- Product ID
- 55315-940_9aa00f88-ff1c-9fc0-e053-2995a90a8264
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- FRED'S INC.
- Application
- ANDA079205
- Marketing category
- ANDA
- Marketing start
- 2017-01-01
- Marketing end
- 2020-08-01
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record