Trandolapril and Verapamil Hydrochloride

Product NDC
59762-0142
Requested package NDC
59762-0142-1
11-digit product format
597620142
Labeler code
59762
Product ID
59762-0142_35f39159-66fa-d915-af29-b37d8f5a7800
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Trandolapril and Verapamil Hydrochloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Greenstone LLC
Application
NDA020591
Marketing category
NDA
Marketing start
2015-02-25
Marketing end
2021-08-14
Substance
TRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE
Active strength
2 mg/1; mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA],Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

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

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage59762-014259762-0142-1DDiscontinued by firm2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 4 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
N020591-001TARKATRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE2MG;180MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-22
N020591-002TARKATRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE4MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-22
N020591-003TARKATRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE1MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET, EXTENDED RELEASE / ORALRLD1996-10-22
N020591-004TARKATRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE2MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-22

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.

Product history page 1 of 5 · 172 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08N020591-001TARKA2MG;180MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-2284e616aacf4f…
2026-09-14 22:38:342026-08N020591-002TARKA4MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-2284e616aacf4f…
2026-09-14 22:38:342026-08N020591-003TARKA1MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET, EXTENDED RELEASE / ORALRLD1996-10-2284e616aacf4f…
2026-09-14 22:38:342026-08N020591-004TARKA2MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-2284e616aacf4f…
2026-08-18 06:07:402026-07N020591-001TARKA2MG;180MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-22caaa826d4ba7…
2026-08-18 06:07:402026-07N020591-002TARKA4MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-22caaa826d4ba7…
2026-08-18 06:07:402026-07N020591-003TARKA1MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET, EXTENDED RELEASE / ORALRLD1996-10-22caaa826d4ba7…
2026-08-18 06:07:402026-07N020591-004TARKA2MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-22caaa826d4ba7…
2026-02-19 14:30 UTC2026-02N020591-001TARKA2MG;180MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-22011fe1cb6892…
2026-02-19 14:30 UTC2026-02N020591-002TARKA4MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-22011fe1cb6892…
2026-02-19 14:30 UTC2026-02N020591-003TARKA1MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET, EXTENDED RELEASE / ORALRLD1996-10-22011fe1cb6892…
2026-02-19 14:30 UTC2026-02N020591-004TARKA2MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-22011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N020591-001TARKA2MG;180MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-2231067a03dcf5…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N020591-002TARKA4MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-2231067a03dcf5…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N020591-003TARKA1MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET, EXTENDED RELEASE / ORALRLD1996-10-2231067a03dcf5…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N020591-004TARKA2MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-2231067a03dcf5…
2025-08-23 18:47 UTC2025-08N020591-001TARKA2MG;180MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-226a471c1ec25d…
2025-08-23 18:47 UTC2025-08N020591-002TARKA4MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-226a471c1ec25d…
2025-08-23 18:47 UTC2025-08N020591-003TARKA1MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET, EXTENDED RELEASE / ORALRLD1996-10-226a471c1ec25d…
2025-08-23 18:47 UTC2025-08N020591-004TARKA2MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-226a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N020591-001TARKA2MG;180MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-22fd3edfee7708…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N020591-002TARKA4MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-22fd3edfee7708…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N020591-003TARKA1MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET, EXTENDED RELEASE / ORALRLD1996-10-22fd3edfee7708…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N020591-004TARKA2MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-22fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N020591-001TARKA2MG;180MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-22b8a1b40f171c…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N020591-002TARKA4MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-22b8a1b40f171c…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N020591-003TARKA1MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET, EXTENDED RELEASE / ORALRLD1996-10-22b8a1b40f171c…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N020591-004TARKA2MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-22b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N020591-001TARKA2MG;180MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-2203ed91905a0d…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N020591-002TARKA4MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-2203ed91905a0d…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N020591-003TARKA1MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET, EXTENDED RELEASE / ORALRLD1996-10-2203ed91905a0d…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N020591-004TARKA2MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-2203ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N020591-001TARKA2MG;180MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-222680178bc6a6…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N020591-002TARKA4MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-222680178bc6a6…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N020591-003TARKA1MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET, EXTENDED RELEASE / ORALRLD1996-10-222680178bc6a6…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N020591-004TARKA2MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-222680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N020591-001TARKA2MG;180MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-225bbf6a4d5a75…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N020591-002TARKA4MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-225bbf6a4d5a75…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N020591-003TARKA1MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET, EXTENDED RELEASE / ORALRLD1996-10-225bbf6a4d5a75…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N020591-004TARKA2MG;240MGTABLET, EXTENDED RELEASE / ORALRLD1996-10-225bbf6a4d5a75…

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2019-12-13 00:20 UTC2019-12N020591-001AB174a2ff9319b5…
2019-12-13 00:20 UTC2019-12N020591-002AB174a2ff9319b5…
2019-12-13 00:20 UTC2019-12N020591-004AB174a2ff9319b5…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05N020591-001AB187673890dc5c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05N020591-002AB187673890dc5c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05N020591-004AB187673890dc5c…
2021-03-12 10:30 UTC2021-03N020591-001AB15aa47cf7b7d7…
2021-03-12 10:30 UTC2021-03N020591-002AB15aa47cf7b7d7…
2021-03-12 10:30 UTC2021-03N020591-004AB15aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12N020591-001AB18869cabd3fbd…
2020-12-22 03:56 UTC2020-12N020591-002AB18869cabd3fbd…
2020-12-22 03:56 UTC2020-12N020591-004AB18869cabd3fbd…
2020-11-12 02:37 UTC2020-11N020591-001AB1c0c555d07b60…
2020-11-12 02:37 UTC2020-11N020591-002AB1c0c555d07b60…
2020-11-12 02:37 UTC2020-11N020591-004AB1c0c555d07b60…
2019-12-14 00:12 UTC2019-12N020591-001AB13f01610625f2…
2019-12-14 00:12 UTC2019-12N020591-002AB13f01610625f2…
2019-12-14 00:12 UTC2019-12N020591-004AB13f01610625f2…
2019-09-15 20:21 UTC2019-09N020591-001AB1b00525d2431f…
2019-09-15 20:21 UTC2019-09N020591-002AB1b00525d2431f…
2019-09-15 20:21 UTC2019-09N020591-004AB1b00525d2431f…
2019-07-19 19:46 UTC2019-07N020591-001AB1ea99ee380514…
2019-07-19 19:46 UTC2019-07N020591-002AB1ea99ee380514…
2019-07-19 19:46 UTC2019-07N020591-003AB1ea99ee380514…
2019-07-19 19:46 UTC2019-07N020591-004AB1ea99ee380514…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59762-0142-1EA - Each59762-01427c002d7f-f2e1-4a1e-81d6-2dfd1c484bf312015-04-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
TRANDOLAPRILACTIVE INGREDIENT1T0N3G9CRCTRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
VERAPAMIL HYDROCHLORIDEACTIVE INGREDIENTV3888OEY5RTRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
TRANDOLAPRILATACTIVE MOIETYRR6866VL0OTRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
VERAPAMILACTIVE MOIETYCJ0O37KU29TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
ALCOHOLINACTIVE INGREDIENT3K9958V90MTRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UTRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
DOCUSATE SODIUMINACTIVE INGREDIENTF05Q2T2JA0TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
FERRIC OXIDE REDINACTIVE INGREDIENT1K09F3G675TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
HYDROXYPROPYL CELLULOSE (TYPE H)INACTIVE INGREDIENTRFW2ET671PTRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOTRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XTRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1ATRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
POVIDONESINACTIVE INGREDIENTFZ989GH94ETRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
SODIUM ALGINATEINACTIVE INGREDIENTC269C4G2ZQTRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
SODIUM STEARYL FUMARATEINACTIVE INGREDIENT7CV7WJK4UITRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJTRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
TALCINACTIVE INGREDIENT7SEV7J4R1UTRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPTRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20
WATERINACTIVE INGREDIENT059QF0KO0RTRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE ER (TRANDOLAPRIL AND VERAPAMIL HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [GREENSTONE LLC]20

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
59762-0142-159762014201100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59762-0142-1) 2015-02-252021-08-14NoNoCurrent