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Diclofenac sodium and Misoprostol - 59762-0029-3 - (Diclofenac sodium and Misoprostol)

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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]

Complete Information of Diclofenac sodium and Misoprostol


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