# Diphenhydramine Hydrochloride

NDC: 76045-235
Generic name: Diphenhydramine Hydrochloride
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20250602

FDA application: ANDA091526

## Active ingredients

- DIPHENHYDRAMINE HYDROCHLORIDE: 50 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76045-235"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76045-235
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6d1aa0e2-036d-4382-a458-fc0300dba7cb