# Meperidine Hydrochloride

NDC: 0054-3545
Generic name: Meperidine Hydrochloride
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 19850130

FDA application: ANDA088744

## Active ingredients

- MEPERIDINE HYDROCHLORIDE: 50 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0054-3545"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0054-3545
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=15bc51a8-1e24-4d33-9a2f-05a41c29acf0