# ALBUTEROL SULFATE

NDC: 70752-102
Generic name: ALBUTEROL SULFATE
Labeler / Manufacturer: QUAGEN PHARMACEUTICALS LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SYRUP
Routes: ORAL
Marketing started: 20190906

FDA application: ANDA212197

## Active ingredients

- ALBUTEROL SULFATE: 2 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70752-102"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70752-102
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=99a490cc-e41d-436b-9cf3-8facb7ac714f