# Atropine Sulfate

NDC: 0517-1001
Generic name: ATROPINE SULFATE
Labeler / Manufacturer: American Regent, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220802

FDA application: ANDA216120

## Active ingredients

- ATROPINE SULFATE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0517-1001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0517-1001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6fee1727-52b7-4f73-ab45-ef47d6a1c5bb