# ALBUTEROL SULFATE

NDC: 51662-1499
Generic name: ALBUTEROL SULFATE
Labeler / Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20200129

FDA application: ANDA074880

## Active ingredients

- ALBUTEROL SULFATE: 2.5 mg/3mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51662-1499"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1499
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9d4ef83f-8ca0-811e-e053-2995a90a6d0d