NDC 68645-130
Fluoxetine 20 mg capsule
On the label: Legacy Pharmaceutical Packaging. It's repackaged: Legacy Pharmaceutical Packaging rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 50111-648.
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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Recalls
- Apr 13, 2015 · Class II · Teva Pharmaceuticals USA
Chemical Contamination: Product recalled due to an elevated level of a residual solvent impurity in the API that exceeds the Threshold of Toxicological Concern (TTC) calculation for the impurity.
Lots: Lot #: 6A207012, Exp 7/2015. - Apr 13, 2015 · Class II · Teva Pharmaceuticals USA
Chemical Contamination: Product recalled due to an elevated level of a residual solvent impurity in the API that exceeds the Threshold of Toxicological Concern (TTC) calculation for the impurity.
Lots: Lot #: a) 6A208123, Exp 8/2015; b) 6A208121, Exp 8/2015. - Feb 14, 2014 · Class II · Legacy Pharmaceutical Packaging
Chemical Contamination: The recalling firm received notice that their supplier is recalling capsules due to complaints of capsules having an unusual odor.
Lots: Lot numbers: 131328, Exp 08/15; 131634, Exp 09/15; and 131833, Exp 11/15 - Feb 12, 2014 · Class II · Teva Pharmaceuticals USA
Chemical Contamination: Recall due to a customer complaint trend regarding capsule odor.
Lots: Lot #: a) 6A211150, 6A211151, 6A211152, 6A211153, 6A211154, Exp 11/15; 6A212083, 6A212084, 6A212085, 6A212086, Exp 12/15; b) 6A211143, 6A211145, 6A211146, 6A211147, Exp 11/15; c) 6A209116, 6A209117, 6A209118, 6A209119, 6A209120, Exp 09/15; 6A211139, 6A211140, 6A211141, Exp 11/15; 6A212087, Exp 12/1… - Feb 12, 2014 · Class II · Teva Pharmaceuticals USA
Chemical Contamination: Recall due to a customer complaint trend regarding capsule odor.
Lots: Lot #: 6A211158, 6A211159, 6A211163, Exp 11/15
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Fluoxetine: every company that makes it
- Form
- capsule, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA076001
- On the market since
- Jan 25, 2011
- Package NDCs
68645-130-54- Official label
- DailyMed (National Library of Medicine), updated Mar 3, 2026
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