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ARTHROTEC
ARTHROTEC - 63629-3359-2 - (diclofenac sodium and misoprostol)
Drug Information of ARTHROTEC
| Product NDC: | 63629-3359 |
| Proprietary Name: | ARTHROTEC |
| Non Proprietary Name: | diclofenac sodium and misoprostol |
| Active Ingredient(s): | 75; 200 mg/1; ug/1 & nbsp; diclofenac sodium and misoprostol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ARTHROTEC
| Product NDC: | 63629-3359 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020607 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19971224 |
Package Information of ARTHROTEC
| Package NDC: | 63629-3359-2 |
| Package Description: | 120 TABLET, FILM COATED in 1 BOTTLE (63629-3359-2) |
NDC Information of ARTHROTEC
| NDC Code | 63629-3359-2 |
| Proprietary Name | ARTHROTEC |
| Package Description | 120 TABLET, FILM COATED in 1 BOTTLE (63629-3359-2) |
| Product NDC | 63629-3359 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | diclofenac sodium and misoprostol |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19971224 |
| Marketing Category Name | NDA |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | DICLOFENAC SODIUM; MISOPROSTOL |
| Strength Number | 75; 200 |
| Strength Unit | mg/1; ug/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC],Prostaglandin E1 Analog [EPC],Prostaglandins E, Synthetic [Chemical/Ingredient] |
