Ibuprofen 50090-7283
Product NDC
50090-7283- Manufacturer
- A-S Medication Solutions
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 23, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA202413
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ibuprofen | 800 mg/1 |
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]
Packaging Options(9)
10 TABLET, FILM COATED in 1 BOTTLE (50090-7283-0)
15 TABLET, FILM COATED in 1 BOTTLE (50090-7283-1)
30 TABLET, FILM COATED in 1 BOTTLE (50090-7283-2)
45 TABLET, FILM COATED in 1 BOTTLE (50090-7283-3)
60 TABLET, FILM COATED in 1 BOTTLE (50090-7283-4)
100 TABLET, FILM COATED in 1 BOTTLE (50090-7283-5)
21 TABLET, FILM COATED in 1 BOTTLE (50090-7283-7)
12 TABLET, FILM COATED in 1 BOTTLE (50090-7283-8)
40 TABLET, FILM COATED in 1 BOTTLE (50090-7283-9)