# Oxacillin

NDC: 64679-698
Generic name: Oxacillin
Labeler / Manufacturer: Wockhardt USA LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20170731

FDA application: ANDA207147

## Active ingredients

- OXACILLIN SODIUM: 1 g/20mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"64679-698"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64679-698
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=195c2054-0746-421d-8b20-8c751bdd772b