# AMPICILLIN

NDC: 71872-7204
Generic name: Ampicillin Injection
Labeler / Manufacturer: Medical Purchasing Solutions, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20190306

FDA application: ANDA090354

## Active ingredients

- AMPICILLIN SODIUM: 1 g/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71872-7204"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71872-7204
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9f1a0a45-a38a-0df0-e053-2995a90a539c