NDC 12634-260
Hydrocodone Bitartrate And Acetaminophen 325 mg / 7.5 mg tablet
On the label: Apotheca, Inc.. It's repackaged from NDC 57664-170, made by Sun Pharmaceutical Industries, Inc. (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 and 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 Apotheca, Inc. names for other drugs.
Product details
- Generic drug
- Acetaminophen and Hydrocodone: every company that makes it
- Form
- tablet
- Strength
- 325 mg / 7.5 mg
- Approval
- ANDA ANDA090118
- On the market since
- Mar 30, 2009
- Package NDCs
12634-260-0012634-260-4012634-260-5012634-260-5512634-260-6612634-260-7112634-260-7912634-260-8012634-260-8512634-260-9112634-260-94- Official label
- DailyMed (National Library of Medicine), updated Jun 10, 2016
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?