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"71335-1183-2" National Drug Code (NDC)
Diclofenac Sodium And Misoprostol 14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-2)
(Bryant Ranch Prepack)
NDC Code
71335-1183-2
Package Description
14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-2)
Product NDC
71335-1183
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
20161201
Marketing Category Name
ANDA
Application Number
ANDA203995
Manufacturer
Bryant Ranch Prepack
Substance Name
DICLOFENAC SODIUM; MISOPROSTOL
Strength
75; 200
Strength Unit
mg/1; ug/1
Pharmacy Classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], 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/71335-1183-2