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"0591-0339-05" National Drug Code (NDC)
Diclofenac Sodium 12 BOTTLE, PLASTIC in 1 BOX (0591-0339-05) > 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
(Watson Pharma, Inc.)
NDC Code
0591-0339-05
Package Description
12 BOTTLE, PLASTIC in 1 BOX (0591-0339-05) > 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
Product NDC
0591-0339
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
End Marketing Date
20150228
Marketing Category Name
ANDA
Application Number
ANDA075185
Manufacturer
Watson Pharma, Inc.
Substance Name
DICLOFENAC SODIUM
Strength
75
Strength Unit
mg/1
Pharmacy Classes
Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0591-0339-05