# TRAMADOL HYDROCHLORIDE

NDC: 27808-301
Generic name: TRAMADOL HYDROCHLORIDE
Labeler / Manufacturer: Cranbury Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20241222

FDA application: ANDA091498

## Active ingredients

- TRAMADOL HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"27808-301"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=27808-301
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1d4af58f-17f3-4cbd-870c-098ace954872