# Diphenoxylate Hydrochloride and Atropine Sulfate

NDC: 68788-8090
Generic name: diphenoxylate hydrochloride and atropine sulfate
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20211006

FDA application: ANDA213413

## Active ingredients

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

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-8090"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8090
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=46d5b27b-a710-4767-b308-4f673ddb354c