# hydrocodone bitartrate and acetaminophen

NDC: 27808-130
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: 300 mg/15mL
- HYDROCODONE BITARTRATE: 10 mg/15mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"27808-130"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=27808-130
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=93b6dfdf-ba6e-4ea6-ab85-5ac121e33101