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"68071-3132-4" National Drug Code (NDC)
Diclofenac Sodium 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3132-4)
(NuCare Pharmaceuticals, Inc.)
NDC Code
68071-3132-4
Package Description
14 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3132-4)
Product NDC
68071-3132
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Diclofenac Sodium
Non-Proprietary Name
Diclofenac Sodium
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
19951130
Marketing Category Name
ANDA
Application Number
ANDA074394
Manufacturer
NuCare Pharmaceuticals, Inc.
Substance Name
DICLOFENAC SODIUM
Strength
75
Strength Unit
mg/1
Pharmacy Classes
Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68071-3132-4