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Diclofenac Sodium and Misoprostol - 64679-215-04 - (Diclofenac Sodium and Misoprostol)

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Drug Information of Diclofenac Sodium and Misoprostol

Product NDC: 64679-215
Proprietary Name: Diclofenac Sodium and Misoprostol
Non Proprietary Name: Diclofenac Sodium and Misoprostol
Active Ingredient(s): 50; .2    mg/1; mg/1 & nbsp;   Diclofenac Sodium and Misoprostol
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Diclofenac Sodium and Misoprostol

Product NDC: 64679-215
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201948
Marketing Category: ANDA
Start Marketing Date: 20120815

Package Information of Diclofenac Sodium and Misoprostol

Package NDC: 64679-215-04
Package Description: 10 BLISTER PACK in 1 CARTON (64679-215-04) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of Diclofenac Sodium and Misoprostol

NDC Code 64679-215-04
Proprietary Name Diclofenac Sodium and Misoprostol
Package Description 10 BLISTER PACK in 1 CARTON (64679-215-04) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 64679-215
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diclofenac Sodium and Misoprostol
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20120815
Marketing Category Name ANDA
Labeler Name Wockhardt USA LLC.
Substance Name DICLOFENAC SODIUM; MISOPROSTOL
Strength Number 50; .2
Strength Unit mg/1; mg/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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