NDC 10544-121
Isoniazid 300 mg tablet
On the label: Blenheim Pharmacal, Inc.. It's repackaged: Blenheim Pharmacal, Inc. rebottles it from VersaPharm Incorporated's NDC 61748-013.
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 VersaPharm Incorporated names for other drugs.
Repackaging site
- Blenheim Pharmacal, Inc., North Blenheim, New York, United States · repackages it
Recalls
- May 20, 2014 · Class II · West-Ward Pharmaceutical Corp.
Failed Dissolution Specifications: Stability lots cannot support dissolution past the 36 month time point.
Lots: Lot #: a) 67839A, 67839D, Exp 05/14; 67936A, Exp 02/15; b) 67839B, 67840C, Exp 05/14; 67936B, Exp 02/15; c) 67840A, Exp 05/14; d) 67840B, Exp 05/14; e) 67839C, Exp 05/14 - Dec 4, 2012 · Class II · West-ward Pharmaceutical Corp.
Failed Dissolution Specifications; 36 month stability timepoint
Lots: 67079A; 67079B; 67079C
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Isoniazid: every company that makes it
- Form
- tablet
- Strength
- 300 mg
- Approval
- ANDA ANDA087425
- On the market since
- Jun 28, 2013
- Package NDCs
10544-121-30- Official label
- DailyMed (National Library of Medicine), updated Mar 16, 2015
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