Diclofenac Sodium - Diclofenac Sodium
Navigation: NDC > Supplier starting with: W > WATSON PHARMA, INC.| Field | Value |
|---|---|
| NDC Code: | 0591-0339 |
| Proprietary Name: | Diclofenac Sodium |
| Suffix: | Delayed Release |
| Non-Proprietary Name: | Diclofenac Sodium |
| Dosage Form: | TABLET, DELAYED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 13-11-1998 |
| End of Marketing: | 28-02-2015 |
| Category Name: | ANDA |
| Application Number: | ANDA075185 |
| Labeler: | WATSON PHARMA, INC. |
| Substance Name: | DICLOFENAC SODIUM |
| Active Numerator Strength: | 75 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
| DEA Schedule: |