# Diphenoxylate Hydrochloride and Atropine Sulfate

NDC: 62559-490
Generic name: Diphenoxylate Hydrochloride and Atropine Sulfate
Labeler / Manufacturer: ANI Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170707

FDA application: ANDA086727

## 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:"62559-490"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62559-490
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=73dc5f91-d562-44c5-a556-66c96ed1dd82