NDC 11534-201
Sulfasalazine 500 mg tablet, delayed release
On the label: Sunrise Pharmaceutical, Inc..
Where it's made
This label doesn't name the factory that makes the drug (it lists 1 site that tests it, packages it and labels it). 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 Sunrise Pharmaceutical, Inc. names for other drugs.
Product details
- Generic drug
- Sulfasalazine: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA075339
- On the market since
- Dec 11, 2025
- Package NDCs
11534-201-0111534-201-07- Official label
- DailyMed (National Library of Medicine), updated Dec 11, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?