# ATROPINE SULFATE

NDC: 71872-7298
Generic name: ATROPINE SULFATE
Labeler / Manufacturer: Medical Purchasing Solutions, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20210730

FDA application: ANDA212868

## 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:"71872-7298"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71872-7298
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fa1c953b-723b-1abe-e053-6394a90a967f