Ibuprofen 68071-3778
Product NDC
68071-3778- Manufacturer
- Nucare Pharmaceuticals, Inc.
- 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 | 600 mg/1 |
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]
Packaging Options(3)
20 TABLET, FILM COATED in 1 BOTTLE (68071-3778-2)
30 TABLET, FILM COATED in 1 BOTTLE (68071-3778-3)
50 TABLET, FILM COATED in 1 BOTTLE (68071-3778-5)