Ibuprofen 71335-2068
Product NDC
71335-2068- Manufacturer
- Bryant Ranch Prepack
- 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(10)
90 TABLET, FILM COATED in 1 BOTTLE (71335-2068-0)
20 TABLET, FILM COATED in 1 BOTTLE (71335-2068-1)
15 TABLET, FILM COATED in 1 BOTTLE (71335-2068-2)
30 TABLET, FILM COATED in 1 BOTTLE (71335-2068-3)
100 TABLET, FILM COATED in 1 BOTTLE (71335-2068-4)
60 TABLET, FILM COATED in 1 BOTTLE (71335-2068-5)
50 TABLET, FILM COATED in 1 BOTTLE (71335-2068-6)
40 TABLET, FILM COATED in 1 BOTTLE (71335-2068-7)
10 TABLET, FILM COATED in 1 BOTTLE (71335-2068-8)
56 TABLET, FILM COATED in 1 BOTTLE (71335-2068-9)