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"71335-2441-2" National Drug Code (NDC)
Diclofenac Sodium Misoprostol 14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2441-2)
(Bryant Ranch Prepack)
NDC Code
71335-2441-2
Package Description
14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2441-2)
Product NDC
71335-2441
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Diclofenac Sodium Misoprostol
Non-Proprietary Name
Diclofenac Sodium And Misoprostol
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20210715
Marketing Category Name
ANDA
Application Number
ANDA205143
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/71335-2441-2