Ibuprofen 51672-2130
Product NDC
51672-2130- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Suspension
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- June 27, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA209207
Active Ingredients
| Ingredient | Strength |
|---|---|
| Ibuprofen | 100 mg/5mL |
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]
Packaging Options(2)
1 BOTTLE in 1 CARTON (51672-2130-1) / 240 mL in 1 BOTTLE
1 BOTTLE in 1 CARTON (51672-2130-8) / 120 mL in 1 BOTTLE