# Acetaminophen and Codeine Phosphate

NDC: 68071-5010
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: 20130415

FDA application: ANDA202800

## 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:"68071-5010"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-5010
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8f12016d-904f-00b4-e053-2a95a90ad02a