# Butalbital and Acetaminophen

NDC: 68047-753
Generic name: butalbital and acetaminophen
Labeler / Manufacturer: Larken Laboratories, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20151204

FDA application: ANDA203484

## Active ingredients

- ACETAMINOPHEN: 325 mg/1
- BUTALBITAL: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68047-753"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68047-753
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=326c83fc-afed-45ad-9c87-f47968fa1d2a