Ibuprofen 71335-1517
Product NDC
71335-1517- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 30, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA090796
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ibuprofen | 400 mg/1 |
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]
Packaging Options(9)
20 TABLET, FILM COATED in 1 BOTTLE (71335-1517-1)
30 TABLET, FILM COATED in 1 BOTTLE (71335-1517-2)
40 TABLET, FILM COATED in 1 BOTTLE (71335-1517-3)
60 TABLET, FILM COATED in 1 BOTTLE (71335-1517-4)
90 TABLET, FILM COATED in 1 BOTTLE (71335-1517-5)
120 TABLET, FILM COATED in 1 BOTTLE (71335-1517-6)
100 TABLET, FILM COATED in 1 BOTTLE (71335-1517-7)
21 TABLET, FILM COATED in 1 BOTTLE (71335-1517-8)
15 TABLET, FILM COATED in 1 BOTTLE (71335-1517-9)