# butalbital and acetaminophen

NDC: 0603-2540
Generic name: butalbital and acetaminophen
Labeler / Manufacturer: Endo USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19990603

FDA application: ANDA089987

## Active ingredients

- ACETAMINOPHEN: 325 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:"0603-2540"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0603-2540
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e619b656-4123-4878-b601-b0edad3c428b