# Ampicillin

NDC: 0781-9413
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: INTRAVENOUS
Marketing started: 19870219

FDA application: ANDA062738

## 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:"0781-9413"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-9413
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f77db491-31c4-4a7c-a114-0f3244c97090