NDC Code | 80425-0414-3 |
Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0414-3) |
Product NDC | 80425-0414 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Diclofenac Sodium |
Non-Proprietary Name | Diclofenac Sodium |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20240711 |
Marketing Category Name | ANDA |
Application Number | ANDA216275 |
Manufacturer | Advanced Rx of Tennessee, LLC |
Substance Name | DICLOFENAC SODIUM |
Strength | 100 |
Strength Unit | mg/1 |
Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC] |