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"71335-0481-6" National Drug Code (NDC)
Diclofenac Sodium 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-6)
(Bryant Ranch Prepack)
NDC Code
71335-0481-6
Package Description
1000 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-6)
Product NDC
71335-0481
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Diclofenac Sodium
Proprietary Name Suffix
Delayed Release
Non-Proprietary Name
Diclofenac Sodium
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
19981113
Marketing Category Name
ANDA
Application Number
ANDA075185
Manufacturer
Bryant Ranch Prepack
Substance Name
DICLOFENAC SODIUM
Strength
50
Strength Unit
mg/1
Pharmacy Classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-0481-6