Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 16729-0182-01 recalled?

Hydrochlorothiazide · 100 TABLET in 1 BOTTLE (16729-182-01)

Yes — this exact package was recalled

2 FDA recalls name the code 16729-0182-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
Hydrochlorothiazide
Strength
HYDROCHLOROTHIAZIDE 12.5 mg/1
Form
Tablet · Oral
Labeler
Accord Healthcare Inc.
Type
Human Prescription Drug
Product code
16729-0182

Recalls naming this package

Class I · High risk

Hydrochlorothiazide Tablets USP

Product Mix-Up: customer complaint that a sealed bottle labeled as Hydrochlorothiazide Tablets USP 12.5 mg contained only Spironolactone Tablets USP 25 mg.

Terminated Labeling / mix-up Accord Healthcare, Inc. NDC 16729-182-01 D-1206-2018
Class II · Moderate risk

HYDROCHLOROTHIAZIDE Tablet

Labeling: Label Mixup; HYDROCHLOROTHIAZIDE Tablet, 12.5 mg may be potentially mislabeled as chlordiazePOXIDE HCl, Capsule, 25 mg, NDC 00555015902, Pedigree: AD46333_4, EXP: 5/16/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-525-2014

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler