# Atropine Sulfate

NDC: 70069-641
Generic name: Atropine Sulfate
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: INTRAVENOUS
Marketing started: 20240704

FDA application: ANDA215969

## Active ingredients

- ATROPINE SULFATE: 1 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-641"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-641
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a6fac578-c7bc-4b3c-a454-7889cc819118