# Hydrocodone Bitartrate and Acetaminophen

NDC: 27808-036
Generic name: Hydrocodone Bitartrate and Acetaminophen
Labeler / Manufacturer: Cranbury Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20141006

FDA application: ANDA202214

## Active ingredients

- ACETAMINOPHEN: 325 mg/1
- HYDROCODONE BITARTRATE: 7.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"27808-036"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=27808-036
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d4caec6d-4af2-4f1c-9add-c0c948b83b16