NDC 12634-616
Hydrocodone Bitartrate and Acetaminophen 325 mg per 120 mL / 7.5 mg per 120 mL solution
On the label: Apotheca, 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 repackages 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 Apotheca, Inc. names for other drugs.
Product details
- Generic drug
- Acetaminophen and Hydrocodone: every company that makes it
- Form
- solution
- Strength
- 325 mg per 120 mL / 7.5 mg per 120 mL
- Approval
- ANDA ANDA040838
- On the market since
- Mar 31, 2014
- Package NDCs
12634-616-04- Official label
- DailyMed (National Library of Medicine), updated Oct 22, 2014
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