# Theophylline

NDC: 70095-018
Generic name: Theophylline
Labeler / Manufacturer: Sun Pharmaceutical Industries Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20240322

FDA application: ANDA214806

## Active ingredients

- THEOPHYLLINE ANHYDROUS: 450 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70095-018"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70095-018
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=417c9df3-ed15-40ea-a653-b0442f367a54