# Acetylcysteine

NDC: 63323-690
Generic name: ACETYLCYSTEINE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL, RESPIRATORY (INHALATION)
Marketing started: 20120901

FDA application: ANDA203853

## Active ingredients

- ACETYLCYSTEINE: 200 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-690"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-690
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=75b48fab-cef6-465c-a1e0-d085b3988bc4