NDC 67544-848
Fluoxetine Hydrochloride 20 mg capsule
On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged from NDC 0781-2822, made by Sandoz Inc (Fluoxetine 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 (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 Aphena Pharma Solutions - Tennessee, Inc. names for other drugs.
Product details
- Generic drug
- Fluoxetine: every company that makes it
- Form
- capsule
- Strength
- 20 mg
- Approval
- ANDA ANDA075049
- On the market since
- Jan 29, 2002
- Package NDCs
67544-848-3067544-848-4567544-848-5367544-848-6067544-848-7067544-848-8067544-848-92- Official label
- DailyMed (National Library of Medicine), updated Jun 30, 2014
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?