NDC 63739-014
Diltiazem Hydrochloride Extended-Release 120 mg capsule, coated, extended release
On the label: McKesson Packaging Services Business Unit of McKesson Corporation. It's repackaged: McKesson Packaging Services Business Unit of McKesson Corporation rebottles it from ENDO USA, Inc.'s NDC 10370-829.
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 ENDO USA, Inc. names for other drugs.
Repackaging site
- Legacy Pharmaceutical Packaging, Location not on file · repackages it and relabels it
Recalls
- Apr 23, 2018 · Class III · Mckesson Packaging Services
Failed Dissolution Specifications. High dissolution results were obtained during stability testing.
Lots: Lot #: 0115086, Exp. 12/2018
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Diltiazem: every company that makes it
- Form
- capsule, coated, extended release
- Strength
- 120 mg
- Approval
- ANDA ANDA074984
- On the market since
- Oct 1, 2015
- Package NDCs
63739-014-10- Official label
- DailyMed (National Library of Medicine), updated Aug 23, 2024
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