# Atropine Sulfate

NDC: 0404-9802
Generic name: Atropine Sulfate
Labeler / Manufacturer: Henry Schein, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20240822

FDA application: ANDA216120

## Active ingredients

- ATROPINE SULFATE: .4 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0404-9802"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0404-9802
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b753894e-81f8-4e81-b07a-c338311ded5b