Hydrochlorothiazide

Product NDC
69367-219
11-digit product format
693670219
Labeler code
69367
Product ID
69367-219_9fe99531-f04b-447d-bc2b-61177b064d9e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydrochlorothiazide
Dosage form
CAPSULE
Route
ORAL
Labeler
Westminster Pharmaceuticals, LLC
Application
ANDA203561
Marketing category
ANDA
Marketing start
2019-06-07
Substance
HYDROCHLOROTHIAZIDE
Active strength
12.5 mg/1
Pharmacologic classes
Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Orange Book products#

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A203561-001HYDROCHLOROTHIAZIDEHYDROCHLOROTHIAZIDE12.5MGCAPSULE / ORALAB2019-01-14

Therapeutic equivalence codes#

Application-product, TE code table
Application-productTE code
A203561-001AB

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
HydrochlorothiazideHYDROCHLOROTHIAZIDEWestminster Pharmaceuticals, LLC0fc94bc2-fa38-439a-a609-1b4130cdacb12026-03-17Warnings, Adverse reactionsExact identifier

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings

WARNINGS Acute Myopia and Secondary Angle-Closure Glaucoma Hydrochlorothiazide, a sulfonamide, can cause an idiosyncratic reaction, resulting in acute transient myopia and acute angle-closure glaucoma. Symptoms include acute onset of decreased visual acuity or ocular pain and typically occur within hours to weeks of drug initiation. Untreated acute angle-closure glaucoma can lead to permanent vision loss. The primary treatment is to discontinue hydrochlorothiazide as rapidly as possible. Prompt medical or surgical treatments may need to be considered if the intraocular pressure remains uncontrolled. Risk factors for developing acute angle-closure glaucoma may include a history of sulfonamide or penicillin allergy. Diabetes and Hypoglycemia Latent diabetes mellitus may become manifest and diabetic patients given thiazides may require adjustment of their insulin dose. Renal Disease Cumulative effects of the thiazides may develop in patients with impaired renal function. In such patients, thiazides may precipitate azotemia.

Adverse reactions cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

adverse reactions

ADVERSE REACTIONS The adverse reactions associated with hydrochlorothiazide have been shown to be dose related. In controlled clinical trials, the adverse events reported with doses of 12.5 mg hydrochlorothiazide once daily were comparable to placebo. The following adverse reactions have been reported for doses of hydrochlorothiazide 25 mg and greater and, within each category, are listed in the order of decreasing severity. Body as a whole: Weakness. Cardiovascular: Hypotension including orthostatic hypotension (may be aggravated by alcohol, barbiturates, narcotics or antihypertensive drugs). Digestive: Pancreatitis, jaundice (intrahepatic cholestatic jaundice), diarrhea, vomiting, sialadenitis, cramping, constipation, gastric irritation, nausea, anorexia. Hematologic: Aplastic anemia, agranulocytosis, leukopenia, hemolytic anemia, thrombocytopenia. Hypersensitivity: Anaphylactic reactions, necrotizing angiitis (vasculitis and cutaneous vasculitis), respiratory distress including pneumonitis and pulmonary edema, photosensitivity, fever, urticaria, rash, purpura. Metabolic: Electrolyte imbalance (see PRECAUTIONS ), hyperglycemia, glycosuria, hyperuricemia. Musculoskeletal: Muscle spasm. Nervous System/Psychiatric: Vertigo, paresthesia, dizziness, headache, restlessness. Renal: Renal failure, renal dysfunction, interstitial nephritis (see WARNINGS ). Skin: Erythema multiforme including Stevens-Johnson syndrome, exfoliative dermatitis including toxic epidermal necrolysis, alopecia. Special Senses: Transient blurred vision, xanthopsia. Urogenital: Impotence. Whenever adverse reactions are moderate or severe, thiazide dosage should be reduced or therapy withdrawn. Postmarketing Experience The following adverse reaction has been identified during post-approval use of hydrochlorothiazide. Because the reaction is reported voluntarily from a population of uncertain size, it is not possible to reliably estimate the frequency or establish a causal relationship to drug exposure. Non-melanoma Skin Cancer Hydrochlorothiazide is associated with an increased risk of non-melanoma skin cancer. In a study conducted in the Sentinel System, increased risk was predominantly for squamous cell carcinoma (SCC) and in white patients taking large cumulative doses. The increased risk for SCC in the overall population was approximately 1 additional case per 16,000 patients per year,...

Additional Listing Data#

Finished product
Yes
Brand name base
Hydrochlorothiazide
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HYDROCHLOROTHIAZIDE12.5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii0J48LPH2TH
Rxcui199903

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c19ec24d-2c40-4b8d-7c20-500ffa3660a1Product name320260303
1199f4b7-b537-466c-9a1c-cb09131e9f8bProduct name120251117
e1a63b6e-1877-c2c1-01a3-03ea2817aa6fProduct name320251027
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96816964-c075-ffa7-b7b8-d8570411a3b9Product name720250305
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
162cbc9d-ecc3-72ba-af9f-c76e2756ef54Product name320221207
9b303cd4-3186-2454-5706-3137e8b2dfd2Product name420221110
47fc2fe9-7afb-4be9-989d-787aaa6ad0eaProduct name120200505
a8e65197-7914-7acf-c7ec-914d53819b34Product name320190624
8b67f333-47d1-8464-7ce4-406d3dbb295fProduct name720190618
89a57420-ab44-5323-14f9-595159145f9bProduct name220190612
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7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
00fc2cf9-672f-3e0b-6afa-43cbc864d058Product name420180613
15b375b1-89c7-9594-80df-5a8c8864aee0Product name320180108
a7349398-661d-d9fc-46df-7e128bbd61d9Product name520171113
1bdb87cf-9b1f-6a51-5eb7-d182aaffaa3dProduct name220170719
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55bffd21-17e1-ff02-2e8f-1f9a532b9502Product name220150320
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041df61b-f8b6-48a6-7b67-411e1412678bProduct name120140508
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df89bd47-2db4-d593-ab37-d11953fd5536Product name120140508
f151007d-265d-9fbe-857d-1d44f1cb76baProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69367-219-01Hydrochlorothiazide100 in 1 BOTTLE, PLASTICCAPSULE1005
69367-219-05Hydrochlorothiazide500 in 1 BOTTLE, PLASTICCAPSULE5005
69367-219-10Hydrochlorothiazide1000 in 1 BOTTLE, PLASTICCAPSULE10005

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69367-219-01EA - Each69367-219c8a98182-a94b-4341-ab17-3e10a5dd6c9612019-07-02
69367-219-05EA - Each69367-219c78504a2-8374-4801-b908-55647a266f3112019-07-02
69367-219-10EA - Each69367-219d77fb33c-8b3e-4bf9-a9c6-e0fb1477313d12019-07-02

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69367-219HYDROCHLOROTHIAZIDE CAPSULE [WESTMINSTER PHARMACEUTICALS]3Current NDC, Legacy NDC, 3 package rows20210114_0fc94bc2-fa38-439a-a609-1b4130cdacb1.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
199903hydroCHLOROthiazide 12.5 MG Oral CapsulePSN0fc94bc2-fa38-439a-a609-1b4130cdacb15
199903hydrochlorothiazide 12.5 MG Oral CapsuleSCD0fc94bc2-fa38-439a-a609-1b4130cdacb15
199903HCTZ 12.5 MG Oral CapsuleSY0fc94bc2-fa38-439a-a609-1b4130cdacb15
199903hydroCHLOROthiazide 12.5 MG Oral CapsulePSNb54ec2b1-3325-46a1-b654-8a75dc41ab0a3
199903hydrochlorothiazide 12.5 MG Oral CapsuleSCDb54ec2b1-3325-46a1-b654-8a75dc41ab0a3
199903HCTZ 12.5 MG Oral CapsuleSYb54ec2b1-3325-46a1-b654-8a75dc41ab0a3
199903hydroCHLOROthiazide 12.5 MG Oral CapsulePSN460f922c-1fda-44a5-889e-d7009883176b2
199903hydroCHLOROthiazide 12.5 MG Oral CapsulePSNef56450d-86d3-2654-e053-2995a90a142c2
199903hydrochlorothiazide 12.5 MG Oral CapsuleSCD460f922c-1fda-44a5-889e-d7009883176b2
199903hydrochlorothiazide 12.5 MG Oral CapsuleSCDef56450d-86d3-2654-e053-2995a90a142c2
199903HCTZ 12.5 MG Oral CapsuleSY460f922c-1fda-44a5-889e-d7009883176b2
199903HCTZ 12.5 MG Oral CapsuleSYef56450d-86d3-2654-e053-2995a90a142c2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69367-219-0169367021901100 CAPSULE in 1 BOTTLE, PLASTIC (69367-219-01) 100 capsule2019-06-070000-00-00NoNoCurrent
69367-219-0569367021905500 CAPSULE in 1 BOTTLE, PLASTIC (69367-219-05) 500 capsule2019-06-070000-00-00NoNoCurrent
69367-219-10693670219101000 CAPSULE in 1 BOTTLE, PLASTIC (69367-219-10) 1000 capsule2019-06-070000-00-00NoNoCurrent