# Hydrocodone Bitartrate and Acetaminophen

NDC: 0406-0377
Generic name: Hydrocodone Bitartrate and Acetaminophen
Labeler / Manufacturer: SpecGx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170331

FDA application: ANDA206718

## Active ingredients

- ACETAMINOPHEN: 300 mg/1
- HYDROCODONE BITARTRATE: 7.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0406-0377"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0406-0377
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d621b526-4d9a-48a9-9a3e-d29d6aea2f31