Ibuprofen 71205-0522
Product NDC
71205-0522- Manufacturer
- Proficient Rx Lp
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 24, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA078329
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ibuprofen | 600 mg/1 |
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]
Packaging Options(6)
20 TABLET, FILM COATED in 1 BOTTLE (71205-522-20)
28 TABLET, FILM COATED in 1 BOTTLE (71205-522-28)
30 TABLET, FILM COATED in 1 BOTTLE (71205-522-30)
42 TABLET, FILM COATED in 1 BOTTLE (71205-522-42)
60 TABLET, FILM COATED in 1 BOTTLE (71205-522-60)
90 TABLET, FILM COATED in 1 BOTTLE (71205-522-90)