Ibuprofen 51672-1409
Product NDC
51672-1409- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Suspension
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 23, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA209204
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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 (51672-1409-8) / 118 mL in 1 BOTTLE
473 mL in 1 BOTTLE (51672-1409-9)