# Diphenoxylate Hydrochloride and Atropine Sulfate

NDC: 75826-107
Generic name: Diphenoxylate Hydrochloride and Atropine Sulfate
Labeler / Manufacturer: Winder Laboratories LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220430

FDA application: ANDA211362

## 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:"75826-107"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=75826-107
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7344a2d2-1f8a-4c5a-90e3-181b919c0c7a