# Ampicillin

NDC: 71872-7240
Generic name: Ampicillin
Labeler / Manufacturer: Medical Purchasing Solutions, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20120510

FDA application: ANDA062772

## Active ingredients

- AMPICILLIN SODIUM: 2 g/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71872-7240"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71872-7240
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bbf118c0-7cd3-5a82-e053-2a95a90ac8c8