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Diclofenac Sodium
Diclofenac Sodium - 0781-1381-01 - (Diclofenac Sodium)
Drug Information of Diclofenac Sodium
| Product NDC: | 0781-1381 |
| Proprietary Name: | Diclofenac Sodium |
| Non Proprietary Name: | Diclofenac Sodium |
| Active Ingredient(s): | 100 mg/1 & nbsp; Diclofenac Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diclofenac Sodium
| Product NDC: | 0781-1381 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020254 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19960308 |
Package Information of Diclofenac Sodium
| Package NDC: | 0781-1381-01 |
| Package Description: | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-1381-01) |
NDC Information of Diclofenac Sodium
| NDC Code | 0781-1381-01 |
| Proprietary Name | Diclofenac Sodium |
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-1381-01) |
| Product NDC | 0781-1381 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diclofenac Sodium |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19960308 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Sandoz Inc |
| Substance Name | DICLOFENAC SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
