# MEPERIDINE HYDROCHLORIDE

NDC: 0641-6052
Generic name: MEPERIDINE HYDROCHLORIDE
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 19750122

FDA application: ANDA080445

## Active ingredients

- MEPERIDINE HYDROCHLORIDE: 25 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0641-6052"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0641-6052
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e0e998da-f056-4fce-be8e-ed60cf3b461b