# butalbital and acetaminophen

NDC: 70010-054
Generic name: butalbital and acetaminophen
Labeler / Manufacturer: Granules Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20200120

FDA application: ANDA213115

## 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:"70010-054"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70010-054
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2091c292-b77b-4ce6-8bba-436c74eee3d7