# Theophylline

NDC: 68462-356
Generic name: Theophylline
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20100713

FDA application: ANDA090355

## Active ingredients

- THEOPHYLLINE ANHYDROUS: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68462-356"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-356
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=56fc2167-ceb6-4e3e-8ff7-5e400dfbd533