# Ampicillin

NDC: 0781-9408
Generic name: Ampicillin sodium
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 19710303

FDA application: ANDA061395

## Active ingredients

- AMPICILLIN SODIUM: 2 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-9408"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-9408
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b371e1a5-1fef-4df2-8940-c4fc02b9e2f0