# BUTALBITAL AND ACETAMINOPHEN

NDC: 81005-123
Generic name: butalbital and acetaminophen
Labeler / Manufacturer: Aarkish Pharmaceuticals NJ Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20241203

FDA application: ANDA214955

## Active ingredients

- ACETAMINOPHEN: 300 mg/1
- BUTALBITAL: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"81005-123"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81005-123
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=82fa5151-d5ee-4ad8-ba7c-a2df8a09e1a6