NDC 68151-2875
Loxapine 5 mg capsule
On the label: Carilion Materials Management. It's repackaged: Carilion Materials Management rebottles it from Actavis Pharma, Inc.'s NDC 0591-0369.
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 Actavis Pharma, Inc. names for other drugs.
Repackaging site
- Carilion Materials Management, Roanoke, Virginia, United States · repackages it
Recalls
- Apr 17, 2012 · Class III · Watson Laboratories Inc
Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.
Lots: Lot #s: 107886A, 107887A, 112874A, 144274A, 196483A, 201146A, 217265A, 260747B, 283308A, 313279A, 313279B, 327892A, 327893A, 327894A, 387239A, 387240A, 427259A, 427260A, 456251A. - Apr 17, 2012 · Class III · Watson Laboratories Inc
Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.
Lots: Lot #s: 101696A, 110829A, 123685A, 123687A - Apr 17, 2012 · Class III · Watson Laboratories Inc
Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.
Lots: Lot #s: 104432A, 104433A, 121344A, 127024A, 144290A
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Loxapine: every company that makes it
- Form
- capsule
- Strength
- 5 mg
- Approval
- ANDA ANDA072204
- On the market since
- Jun 15, 1988
- Package NDCs
68151-2875-0- Official label
- DailyMed (National Library of Medicine), updated Feb 4, 2011
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