# ATROPINE SULFATE

NDC: 51662-1619
Generic name: ATROPINE SULFATE
Labeler / Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: ENDOTRACHEAL, INTRAMEDULLARY, INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20221001

FDA application: ANDA213561

## Active ingredients

- ATROPINE SULFATE: .4 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51662-1619"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1619
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e9fd624a-9abd-dfea-e053-2a95a90a8e9d