NDC 0093-3234

Sulfasalazine 500 mg tablet

On the label: Teva Pharmaceuticals USA, Inc..

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Teva Pharmaceuticals USA, Inc. names for other drugs.

Product details

Generic drug
Sulfasalazine: every company that makes it
Form
tablet, oral
Strength
500 mg
Approval
ANDA ANDA085828
On the market since
Dec 15, 2022
Package NDCs
0093-3234-01 0093-3234-05 0093-3234-10
Official label
DailyMed (National Library of Medicine), updated Aug 22, 2023

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