NDC 54868-6306
Bupropion HydrochlorideSR 200 mg tablet, extended release
On the label: Physicians Total Care, Inc.. It's repackaged from NDC 0185-1111, made by Eon Labs, Inc. (Bupropion Hydrochloride). 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. 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 Physicians Total Care, Inc. names for other drugs.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release
- Strength
- 200 mg
- Approval
- ANDA ANDA075932
- On the market since
- Sep 8, 2011
- Package NDCs
54868-6306-0- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2011
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