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Diclofenac sodium and Misoprostol
Diclofenac sodium and Misoprostol - 59762-0029-3 - (Diclofenac sodium and Misoprostol)
Drug Information of Diclofenac sodium and Misoprostol
| Product NDC: | 59762-0029 |
| Proprietary Name: | Diclofenac sodium and Misoprostol |
| 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 Diclofenac sodium and Misoprostol
| Product NDC: | 59762-0029 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020607 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19971224 |
Package Information of Diclofenac sodium and Misoprostol
| Package NDC: | 59762-0029-3 |
| Package Description: | 250 TABLET, FILM COATED in 1 BOTTLE (59762-0029-3) |
NDC Information of Diclofenac sodium and Misoprostol
| NDC Code | 59762-0029-3 |
| Proprietary Name | Diclofenac sodium and Misoprostol |
| Package Description | 250 TABLET, FILM COATED in 1 BOTTLE (59762-0029-3) |
| Product NDC | 59762-0029 |
| 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 AUTHORIZED GENERIC |
| Labeler Name | Greenstone LLC |
| 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] |
