NDC 0121-1008
Acetaminophen and Codeine Phosphate 30 mg per 12.5 mL / 300 mg per 12.5 mL solution
On the label: Pharmaceutical Associates, Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Pharmaceutical Associates, Inc. names for other drugs.
Product details
- Generic drug
- Acetaminophen and Codeine: every company that makes it
- Form
- solution, oral
- Strength
- 30 mg per 12.5 mL / 300 mg per 12.5 mL
- Approval
- ANDA ANDA087508
- On the market since
- Aug 21, 1981
- Package NDCs
0121-1008-120121-1008-40- Official label
- DailyMed (National Library of Medicine), updated Aug 6, 2026
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