NDC 68788-6352
Hydrocodone Bitartrate and Acetaminophen 325 mg per 15 mL / 7.5 mg per 15 mL solution
On the label: Preferred Pharmaceuticals, Inc... It's repackaged from NDC 0121-0772, made by PAI Holdings, LLC dba PAI Pharma (Hydrocodone Bitartrate and Acetaminophen). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that relabels it). 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 Preferred Pharmaceuticals, Inc.. names for other drugs.
Product details
- Generic drug
- Acetaminophen and Hydrocodone: every company that makes it
- Form
- solution
- Strength
- 325 mg per 15 mL / 7.5 mg per 15 mL
- Approval
- ANDA ANDA040838
- On the market since
- Mar 14, 2016
- Package NDCs
68788-6352-1- Official label
- DailyMed (National Library of Medicine), updated Sep 26, 2017
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