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"64679-217-04" National Drug Code (NDC)
Diclofenac Sodium And Misoprostol 10 BLISTER PACK in 1 CARTON (64679-217-04) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
(Wockhardt USA LLC.)
NDC Code
64679-217-04
Package Description
10 BLISTER PACK in 1 CARTON (64679-217-04) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product NDC
64679-217
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Diclofenac Sodium And Misoprostol
Non-Proprietary Name
Diclofenac Sodium And Misoprostol
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20120815
Marketing Category Name
ANDA
Application Number
ANDA201948
Manufacturer
Wockhardt USA LLC.
Substance Name
DICLOFENAC SODIUM; MISOPROSTOL
Strength
75; .2
Strength Unit
mg/1; mg/1
Pharmacy Classes
Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC],Prostaglandin E1 Analog [EPC],Prostaglandins E, Synthetic [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/64679-217-04