# AMPICILLIN

NDC: 23155-914
Generic name: Ampicillin Injection
Labeler / Manufacturer: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20250131

FDA application: ANDA090354

## Active ingredients

- AMPICILLIN SODIUM: 250 mg/250mg

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"23155-914"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-914
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=302e6df7-37c5-4625-8a61-3e2f302addf2