NDC 60760-499
Hydrochlorothiazide 12.5 mg tablet
On the label: St. Mary's Medical Park Pharmacy. It's repackaged: St. Mary's Medical Park Pharmacy rebottles it from Accord Healthcare Inc.'s NDC 16729-182.
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 Accord Healthcare Inc. names for other drugs.
Repackaging site
- St. Mary's Medical Park Pharmacy, Oro Valley, AZ, United States · repackages it and relabels it
Recalls
- Aug 21, 2018 · Class I · Accord Healthcare, Inc.
Product Mix-Up: customer complaint that a sealed bottle labeled as Hydrochlorothiazide Tablets USP 12.5 mg contained only Spironolactone Tablets USP 25 mg.
Lots: Lot: PW05264, Exp. 11/2019
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Hydrochlorothiazide: every company that makes it
- Form
- tablet, oral
- Strength
- 12.5 mg
- Approval
- ANDA ANDA202556
- On the market since
- Oct 27, 2026
- Package NDCs
60760-499-90- Official label
- DailyMed (National Library of Medicine), updated Oct 29, 2026
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