Home NDC 50111-450-88 Trazodone Hydrochloride
Product NDC 50111-450
Requested package NDC 50111-450-88
11-digit product format 501110450
Labeler code 50111
Product ID 50111-450_3313a8d0-eb39-47a4-b476-0973aad30e02
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Trazodone Hydrochloride
Dosage form TABLET
Route ORAL
Labeler Teva Pharmaceuticals USA, Inc.
Application ANDA071525
Marketing category ANDA
Marketing start 2020-03-11
Substance TRAZODONE HYDROCHLORIDE
Active strength 150 mg/1
Pharmacologic classes Serotonin Reuptake Inhibitor [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A071525-001 TRAZODONE HYDROCHLORIDE TRAZODONE HYDROCHLORIDE 150MG TABLET / ORAL AB 1988-03-09
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 1 matching rows.
Application-product, TE code table Application-product TE code A071525-001 AB
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 Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-08-01 22:54:32 2026-06 A071525-001 TRAZODONE HYDROCHLORIDE 150MG TABLET / ORAL AB 1988-03-09 a50c72e98297…
Observed Orange Book normalized TE history# Captured, Edition, Application-product table Captured Edition Application-product TE code Order Source SHA-256 2026-08-01 22:54:32 2026-06 A071525-001 AB 1 a50c72e98297…
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 Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Trazodone Hydrochloride TRAZODONE HYDROCHLORIDE NCS HealthCare of KY, LLC dba Vangard Labs 310c4b81-d2cf-4014-873d-e71d036105de 2026-05-28 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 071525 application number: ANDA071525 Trazodone Hydrochloride TRAZODONE HYDROCHLORIDE AvKARE a382ac4d-9ab9-796a-e053-2a95a90a2c26 2026-01-15 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 071525 application number: ANDA071525 Trazodone Hydrochloride TRAZODONE HYDROCHLORIDE PD-Rx Pharmaceuticals, Inc. 9b022ae9-dd52-43ae-804b-ddf8e7cfd530 2025-10-01 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 071525 application number: ANDA071525 Trazodone Hydrochloride TRAZODONE HYDROCHLORIDE Teva Pharmaceuticals USA, Inc. 4006d439-e2de-4590-82e9-fc9d56e3ec1b 2025-07-09 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 071525 application number: ANDA071525 ndc (product): 50111-450
Additional Listing Data#
Finished product Yes
Brand name base Trazodone Hydrochloride
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TRAZODONE HYDROCHLORIDE 150 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 6E8ZO8LRNM Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 856364 Internal RxNorm lookup 856373 Internal RxNorm lookup 856377 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50111-450-01 Trazodone Hydrochloride 100 in 1 BOTTLE TABLET 100 30 50111-450-02 Trazodone Hydrochloride 500 in 1 BOTTLE TABLET 500 30
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50111-450 TRAZODONE HYDROCHLORIDE TABLET [TEVA PHARMACEUTICALS USA, INC.] 28 Current NDC, Legacy NDC, 2 package rows 20230210_4006d439-e2de-4590-82e9-fc9d56e3ec1b.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Status 50111-450-88 50111045088 23500 TABLET in 1 CONTAINER (50111-450-88) 23500 tablet 20-JUN-25 Current