# Acetylcysteine

NDC: 68462-946
Generic name: Acetylcysteine
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20240925

FDA application: ANDA213693

## Active ingredients

- ACETYLCYSTEINE: 200 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68462-946"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-946
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f811ddfc-d7c1-4637-ae81-80c38a77cb80