# Hydrocodone Bitartrate and Acetaminophen

NDC: 0245-0410
Generic name: Hydrocodone Bitartrate and Acetaminophen
Labeler / Manufacturer: Upsher-Smith Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170327

FDA application: ANDA206484

## Active ingredients

- ACETAMINOPHEN: 325 mg/1
- HYDROCODONE BITARTRATE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0245-0410"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0245-0410
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3aa0b733-b58f-46bd-8e76-37ddf1dc3356