# Ampicillin

NDC: 70860-118
Generic name: ampicillin sodium
Labeler / Manufacturer: Athenex Pharmaceutical Division, LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20180531
Marketing ended: 20260930
FDA application: ANDA201404

## Active ingredients

- AMPICILLIN SODIUM: 10 g/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70860-118"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70860-118
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=06b1c203-600c-4083-986a-d1d471b56e43