# Acetaminophen and Codeine

NDC: 76420-103
Generic name: Acetaminophen and Codeine
Labeler / Manufacturer: Asclemed USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20080529

FDA application: ANDA040779

## Active ingredients

- ACETAMINOPHEN: 300 mg/1
- CODEINE PHOSPHATE: 30 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76420-103"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76420-103
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3f83ba75-9415-4ace-9416-04d666c005a2