# NEOSTIGMINE METHYLSULFATE

NDC: 71872-7322
Generic name: NEOSTIGMINE METHYLSULFATE
Labeler / Manufacturer: Medical Purchasing Solutions, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20170426

FDA application: ANDA208405

## Active ingredients

- NEOSTIGMINE METHYLSULFATE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71872-7322"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71872-7322
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=12f25113-bf55-cee7-e063-6294a90a9d56