# Diphenoxylate Hydrochloride and Atropine Sulfate

NDC: 69315-910
Generic name: diphenoxylate hydrochloride and atropine sulfate
Labeler / Manufacturer: Leading Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200315

FDA application: ANDA213413

## Active ingredients

- ATROPINE SULFATE: .025 mg/1
- DIPHENOXYLATE HYDROCHLORIDE: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69315-910"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69315-910
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1c188bc9-7c21-4717-94a0-cdfb581fb776