Chlorthalidone

Product NDC
63629-6347
Requested package NDC
63629-6347-2
11-digit product format
636296347
Labeler code
63629
Product ID
63629-6347_fec18d79-a58d-4c22-bb64-c390659344b5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
chlorthalidone
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA086831
Marketing category
ANDA
Marketing start
1981-02-26
Marketing end
0000-00-00
Substance
CHLORTHALIDONE
Active strength
25 mg/1
Pharmacologic classes
Thiazide-like Diuretic [EPC],Increased Diuresis [PE]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage63629-634763629-6347-2DDiscontinued by firm2026-07-31

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

Orange Book products#

Current product rows page 1 of 1 · 2 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A086831-001CHLORTHALIDONECHLORTHALIDONE50MGTABLET / ORALABRLD, RS, Approved before 1982
A086831-002CHLORTHALIDONECHLORTHALIDONE25MGTABLET / ORALABRLD, Approved before 1982

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 2 matching rows.

Application-product, TE code table
Application-productTE code
A086831-001AB
A086831-002AB

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-08-01 22:54:322026-06A086831-001CHLORTHALIDONE50MGTABLET / ORALABRLD, RS, Approved before 1982a50c72e98297…
2026-08-01 22:54:322026-06A086831-002CHLORTHALIDONE25MGTABLET / ORALABRLD, Approved before 1982a50c72e98297…

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2026-08-01 22:54:322026-06A086831-001AB1a50c72e98297…
2026-08-01 22:54:322026-06A086831-002AB1a50c72e98297…

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. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 4 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ChlorthalidoneCHLORTHALIDONEPD-Rx Pharmaceuticals, Inc.bb7112ae-3a37-4525-8c7f-c0f4100ffc0a2026-06-12Warnings, Adverse reactionsExact identifier
application applno (ANDA): 086831
application number: ANDA086831
ChlorthalidoneCHLORTHALIDONESafecor Health, LLCe0e316f6-96d1-4a89-a3b9-f4f0b4c9c8332026-04-03Warnings, Adverse reactionsExact identifier
application applno (ANDA): 086831
application number: ANDA086831
ChlorthalidoneCHLORTHALIDONEMylan Pharmaceuticals Inc.15dd224a-87ad-48dc-80b1-e8382a452c4c2026-04-02Warnings, Adverse reactionsExact identifier
application applno (ANDA): 086831
application number: ANDA086831
ChlorthalidoneCHLORTHALIDONEMylan Institutional Inc.193c85ba-43c2-4be2-82cf-7b394a83390e2026-01-20Warnings, Adverse reactionsExact identifier
application applno (ANDA): 086831
application number: ANDA086831

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-6347-26362963470230 TABLET in 1 BOTTLE (63629-6347-2) 30 tablet2015-09-010000-00-00NoNoCurrent