# Hydrocodone Bitartrate and Acetaminophen

NDC: 27808-049
Generic name: Hydrocodone Bitartrate and Acetaminophen
Labeler / Manufacturer: Cranbury Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20211230

FDA application: ANDA201295

## Active ingredients

- ACETAMINOPHEN: 325 mg/15mL
- HYDROCODONE BITARTRATE: 7.5 mg/15mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"27808-049"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=27808-049
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=57e1fe79-eb60-4f4f-bb38-6df0270d408f