Ibuprofen 71205-0787
Product NDC
71205-0787- Manufacturer
- Proficient Rx Lp
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- August 16, 1994
- Listing Expires
- December 31, 2026
- Application
- ANDA072096
Active Ingredients
| Ingredient | Strength |
|---|---|
| Ibuprofen | 200 mg/1 |
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]
Packaging Options(4)
100 TABLET, FILM COATED in 1 BOTTLE (71205-787-00)
30 TABLET, FILM COATED in 1 BOTTLE (71205-787-30)
60 TABLET, FILM COATED in 1 BOTTLE (71205-787-60)
90 TABLET, FILM COATED in 1 BOTTLE (71205-787-90)