Diclofenac Sodium 85509-1201
Product NDC
85509-1201- Manufacturer
- Phoenix Rx Llc
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 19, 2008
- Listing Expires
- December 31, 2027
- Application
- ANDA077863
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Diclofenac Sodium | 75 mg/1 |
Drug Class
Anti-Inflammatory AgentsNon-Steroidal [CS]Cyclooxygenase Inhibitors [MoA]
Packaging Options(3)
30 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1201-3)
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (85509-1201-6)
90 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1201-9)