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"0013-0102-20" National Drug Code (NDC)

Azulfidine 300 TABLET, DELAYED RELEASE in 1 BOTTLE (0013-0102-20)
(Pfizer Laboratories Div Pfizer Inc)

NDC Code0013-0102-20
Package Description300 TABLET, DELAYED RELEASE in 1 BOTTLE (0013-0102-20)
Product NDC0013-0102
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAzulfidine
Proprietary Name SuffixEn-tabs
Non-Proprietary NameSulfasalazine
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date19500620
Marketing Category NameNDA
Application NumberNDA007073
ManufacturerPfizer Laboratories Div Pfizer Inc
Substance NameSULFASALAZINE
Strength500
Strength Unitmg/1
Pharmacy ClassesAminosalicylate [EPC], Aminosalicylic Acids [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0013-0102-20





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