# PRE-PEN

NDC: 49471-001
Generic name: benzylpenicilloyl polylysine
Labeler / Manufacturer: ALK-ABELLO, INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION
Routes: INTRADERMAL, SUBCUTANEOUS
Marketing started: 19740725

FDA application: BLA050114

## Active ingredients

- BENZYLPENICILLOYL POLYLYSINE: 60 umol/.25mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"49471-001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49471-001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2fbcc40c-f102-4abe-bce5-a93de95874fe