# Hydrocodone Bitartrate and Acetaminophen

NDC: 31722-940
Generic name: Hydrocodone Bitartrate and Acetaminophen
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250822

FDA application: ANDA211487

## Active ingredients

- ACETAMINOPHEN: 325 mg/1
- HYDROCODONE BITARTRATE: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-940"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-940
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4d5bfd3a-3793-4d24-aedd-c04fa34ea736