# Albuterol Sulfate

NDC: 68071-3780
Generic name: Albuterol Sulfate
Labeler / Manufacturer: NuCare Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20111205

FDA application: ANDA077839

## 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:"68071-3780"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-3780
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2c3f975c-dbd8-0362-e063-6394a90a16dd