# Diphenoxylate Hydrochloride and Atropine Sulfate

NDC: 0406-1236
Generic name: diphenoxylate hydrochloride and atropine sulfate
Labeler / Manufacturer: SpecGx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20201030

FDA application: ANDA213335

## 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:"0406-1236"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0406-1236
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=24915aa0-1600-44bb-99fc-46529a794124