NDC 72189-266-30
IBUPROFEN 800 mg/1
IBUPROFEN · TABLET, FILM COATED
IBUPROFEN is a tablet, film coated containing ibuprofen at a strength of 800 mg/1. Manufactured by DIRECT RX.
Key Facts
- Brand Name
- IBUPROFEN
- Generic Name
- IBUPROFEN
- NDC Code (Package)
72189-266-30- NDC Code (Product)
72189-266- Manufacturer
- DIRECT RX
- Strength
- 800 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA090796
- Drug Class
- Nonsteroidal Anti-inflammatory Drug [EPC]
- Marketing Start
- 09/16/2021
Recall History
No Recall HistoryView Full Drug Page
IBUPROFEN — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.