# POLYMYXIN B

NDC: 68083-174
Generic name: POLYMYXIN B SULFATE
Labeler / Manufacturer: Gland Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRATHECAL, INTRAVENOUS, OPHTHALMIC
Marketing started: 20160601

FDA application: ANDA207322

## Active ingredients

- POLYMYXIN B SULFATE: 500000 [USP'U]/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68083-174"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68083-174
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dc74dee2-1d0b-4fab-a29b-1755fdb5da75