# Hydrocodone Bitartrate and Acetaminophen

NDC: 10702-191
Generic name: Hydrocodone Bitartrate and Acetaminophen
Labeler / Manufacturer: KVK-Tech, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170622

FDA application: ANDA209037

## Active ingredients

- ACETAMINOPHEN: 325 mg/1
- HYDROCODONE BITARTRATE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"10702-191"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10702-191
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f1063950-b302-4898-81c2-b1626c9c16ef