NDC 71205-774
Gabapentin 800 mg tablet
On the label: Proficient Rx LP. It's repackaged from NDC 69367-135, made by Westminster Pharmaceuticals, LLC (Gabapentin). 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 Proficient Rx LP names for other drugs.
Product details
- Generic drug
- Gabapentin: every company that makes it
- Form
- tablet, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA205101
- On the market since
- Apr 11, 2016
- Package NDCs
71205-774-3071205-774-6071205-774-90- Official label
- DailyMed (National Library of Medicine), updated Mar 1, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?