# TIADYLT ER

NDC: 70771-1035
Generic name: diltiazem hydrochloride
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20171108

FDA application: ANDA206641

## Active ingredients

- DILTIAZEM HYDROCHLORIDE: 120 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70771-1035"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1035
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d88e3546-3984-4dc9-893a-a29e95804550