NDC 0121-4772
Hydrocodone Bitartrate and Acetaminophen 108 mg per 5 mL / 2.5 mg per 5 mL solution
On the label: Pharmaceutical Associates, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma | Greenville, SC, United States | Makes it | No problems foundAug 1, 2025 · 18 inspections, 1 with FDA action |
Product details
- Generic drug
- Acetaminophen and Hydrocodone: every company that makes it
- Form
- solution, oral
- Strength
- 108 mg per 5 mL / 2.5 mg per 5 mL
- Approval
- ANDA ANDA040838
- On the market since
- Jul 29, 2013
- Package NDCs
0121-4772-050121-4772-40- Official label
- DailyMed (National Library of Medicine), updated Feb 2, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?