# ATROPINE SULFATE

NDC: 51662-1626
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, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20230713

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:"51662-1626"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1626
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0060b971-19bd-2849-e063-6294a90afca8