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diclofenac sodium
diclofenac sodium - 21695-038-60 - (diclofenac sodium)
Drug Information of diclofenac sodium
| Product NDC: | 21695-038 |
| Proprietary Name: | diclofenac sodium |
| Non Proprietary Name: | diclofenac sodium |
| Active Ingredient(s): | 50 mg/1 & nbsp; diclofenac sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of diclofenac sodium
| Product NDC: | 21695-038 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074514 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960326 |
Package Information of diclofenac sodium
| Package NDC: | 21695-038-60 |
| Package Description: | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (21695-038-60) |
NDC Information of diclofenac sodium
| NDC Code | 21695-038-60 |
| Proprietary Name | diclofenac sodium |
| Package Description | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (21695-038-60) |
| Product NDC | 21695-038 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | diclofenac sodium |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19960326 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | DICLOFENAC SODIUM |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
