# Ampicillin

NDC: 72603-221
Generic name: ampicillin sodium
Labeler / Manufacturer: NorthStar Rx, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20240301

FDA application: ANDA062719

## Active ingredients

- AMPICILLIN SODIUM: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72603-221"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-221
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6772d650-9814-49e4-a4ec-0b1a97b837d1