# Diphenoxylate Hydrochloride and Atropine Sulfate

NDC: 0054-3194
Generic name: Diphenoxylate Hydrochloride and Atropine Sulfate
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 19820503

FDA application: ANDA087708

## Active ingredients

- ATROPINE SULFATE: .025 mg/5mL
- DIPHENOXYLATE HYDROCHLORIDE: 2.5 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0054-3194"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0054-3194
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=88ed4ccf-9e35-4142-a5eb-d2b5edd36956