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Diclofenac Potassium
Diclofenac Potassium - 21695-838-42 - (Diclofenac Potassium)
Drug Information of Diclofenac Potassium
| Product NDC: | 21695-838 |
| Proprietary Name: | Diclofenac Potassium |
| Non Proprietary Name: | Diclofenac Potassium |
| Active Ingredient(s): | 50 mg/1 & nbsp; Diclofenac Potassium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diclofenac Potassium
| Product NDC: | 21695-838 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075219 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100121 |
Package Information of Diclofenac Potassium
| Package NDC: | 21695-838-42 |
| Package Description: | 42 TABLET, FILM COATED in 1 BOTTLE (21695-838-42) |
NDC Information of Diclofenac Potassium
| NDC Code | 21695-838-42 |
| Proprietary Name | Diclofenac Potassium |
| Package Description | 42 TABLET, FILM COATED in 1 BOTTLE (21695-838-42) |
| Product NDC | 21695-838 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diclofenac Potassium |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100121 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | DICLOFENAC POTASSIUM |
| 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] |
