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"0013-0102-01" National Drug Code (NDC)
Azulfidine 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0013-0102-01)
(Pfizer Laboratories Div Pfizer Inc)
NDC Code
0013-0102-01
Package Description
100 TABLET, DELAYED RELEASE in 1 BOTTLE (0013-0102-01)
Product NDC
0013-0102
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Azulfidine
Proprietary Name Suffix
En-tabs
Non-Proprietary Name
Sulfasalazine
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
19500620
Marketing Category Name
NDA
Application Number
NDA007073
Manufacturer
Pfizer Laboratories Div Pfizer Inc
Substance Name
SULFASALAZINE
Strength
500
Strength Unit
mg/1
Pharmacy Classes
Aminosalicylate [EPC], Aminosalicylic Acids [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0013-0102-01