# Acetaminophen and Codeine Phosphate

NDC: 68071-3798
Generic name: Acetaminophen and Codeine Phosphate
Labeler / Manufacturer: NuCare Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190910

FDA application: ANDA212418

## Active ingredients

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

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-3798"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-3798
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2e88442f-a6a9-a899-e063-6294a90ac08d