Home NDC 55289-787-60 Triazolam
Product NDC 55289-787
Requested package NDC 55289-787-60
11-digit product format 552890787
Labeler code 55289
Product ID 55289-787_dd0471dc-c829-eecd-e053-2995a90aab12
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name triazolam
Dosage form TABLET
Route ORAL
Labeler PD-Rx Pharmaceuticals, Inc.
Application NDA017892
Marketing category NDA AUTHORIZED GENERIC
Marketing start 1982-11-15
Marketing end 0000-00-00
Substance TRIAZOLAM
Active strength 0 mg/1
Pharmacologic classes Benzodiazepine [EPC], Benzodiazepines [CS]
DEA schedule CIV
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record 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 date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
Orange Book products# Current product rows page 1 of 1 · 3 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N017892-001 HALCION TRIAZOLAM 0.25MG TABLET / ORAL AB RLD, RS 1982-11-15 N017892-002 HALCION TRIAZOLAM 0.5MG TABLET / ORAL 1982-11-15 N017892-003 HALCION TRIAZOLAM 0.125MG TABLET / ORAL AB RLD 1985-04-26
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 2 matching rows.
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 4 · 129 observed 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 2026-09-14 22:38:34 2026-08 N017892-001 HALCION 0.25MG TABLET / ORAL AB RLD, RS 1982-11-15 84e616aacf4f…2026-09-14 22:38:34 2026-08 N017892-002 HALCION 0.5MG TABLET / ORAL 1982-11-15 84e616aacf4f…2026-09-14 22:38:34 2026-08 N017892-003 HALCION 0.125MG TABLET / ORAL AB RLD 1985-04-26 84e616aacf4f…2026-08-18 06:07:40 2026-07 N017892-001 HALCION 0.25MG TABLET / ORAL AB RLD, RS 1982-11-15 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N017892-002 HALCION 0.5MG TABLET / ORAL 1982-11-15 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N017892-003 HALCION 0.125MG TABLET / ORAL AB RLD 1985-04-26 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 N017892-001 HALCION 0.25MG TABLET / ORAL AB RLD, RS 1982-11-15 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N017892-002 HALCION 0.5MG TABLET / ORAL 1982-11-15 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N017892-003 HALCION 0.125MG TABLET / ORAL AB RLD 1985-04-26 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N017892-001 HALCION 0.25MG TABLET / ORAL AB RLD, RS 1982-11-15 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N017892-002 HALCION 0.5MG TABLET / ORAL 1982-11-15 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N017892-003 HALCION 0.125MG TABLET / ORAL AB RLD 1985-04-26 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 N017892-001 HALCION 0.25MG TABLET / ORAL AB RLD, RS 1982-11-15 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N017892-002 HALCION 0.5MG TABLET / ORAL 1982-11-15 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N017892-003 HALCION 0.125MG TABLET / ORAL AB RLD 1985-04-26 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N017892-001 HALCION 0.25MG TABLET / ORAL AB RLD, RS 1982-11-15 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N017892-002 HALCION 0.5MG TABLET / ORAL 1982-11-15 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N017892-003 HALCION 0.125MG TABLET / ORAL AB RLD 1985-04-26 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N017892-001 HALCION 0.25MG TABLET / ORAL AB RLD, RS 1982-11-15 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N017892-002 HALCION 0.5MG TABLET / ORAL 1982-11-15 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N017892-003 HALCION 0.125MG TABLET / ORAL AB RLD 1985-04-26 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N017892-001 HALCION 0.25MG TABLET / ORAL AB RLD, RS 1982-11-15 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N017892-002 HALCION 0.5MG TABLET / ORAL 1982-11-15 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N017892-003 HALCION 0.125MG TABLET / ORAL AB RLD 1985-04-26 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N017892-001 HALCION 0.25MG TABLET / ORAL AB RLD, RS 1982-11-15 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N017892-002 HALCION 0.5MG TABLET / ORAL 1982-11-15 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N017892-003 HALCION 0.125MG TABLET / ORAL AB RLD 1985-04-26 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N017892-001 HALCION 0.25MG TABLET / ORAL AB RLD, RS 1982-11-15 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N017892-002 HALCION 0.5MG TABLET / ORAL 1982-11-15 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N017892-003 HALCION 0.125MG TABLET / ORAL AB RLD 1985-04-26 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N017892-001 HALCION 0.25MG TABLET / ORAL AB RLD, RS 1982-11-15 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N017892-002 HALCION 0.5MG TABLET / ORAL 1982-11-15 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N017892-003 HALCION 0.125MG TABLET / ORAL AB RLD 1985-04-26 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 N017892-001 HALCION 0.25MG TABLET / ORAL AB RLD, RS 1982-11-15 d06236e962d9…2024-10-29 15:01 UTC 2024-10 N017892-002 HALCION 0.5MG TABLET / ORAL 1982-11-15 d06236e962d9…2024-10-29 15:01 UTC 2024-10 N017892-003 HALCION 0.125MG TABLET / ORAL AB RLD 1985-04-26 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N017892-001 HALCION 0.25MG TABLET / ORAL AB RLD, RS 1982-11-15 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N017892-002 HALCION 0.5MG TABLET / ORAL 1982-11-15 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N017892-003 HALCION 0.125MG TABLET / ORAL AB RLD 1985-04-26 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 N017892-001 HALCION 0.25MG TABLET / ORAL AB RLD, RS 1982-11-15 301d65b070ca…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 3 · 86 observed states.
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded triazolam ACTIVE INGREDIENT 1HM943223R TRIAZOLAM TABLET [PD-RX PHARMACEUTICALS, INC.] 3 triazolam ACTIVE MOIETY 1HM943223R TRIAZOLAM TABLET [PD-RX PHARMACEUTICALS, INC.] 3 docusate sodium INACTIVE INGREDIENT F05Q2T2JA0 TRIAZOLAM TABLET [PD-RX PHARMACEUTICALS, INC.] 3 FD&C Blue No. 2 INACTIVE INGREDIENT L06K8R7DQK TRIAZOLAM TABLET [PD-RX PHARMACEUTICALS, INC.] 3 lactose INACTIVE INGREDIENT J2B2A4N98G TRIAZOLAM TABLET [PD-RX PHARMACEUTICALS, INC.] 3 magnesium stearate INACTIVE INGREDIENT 70097M6I30 TRIAZOLAM TABLET [PD-RX PHARMACEUTICALS, INC.] 3 powdered cellulose INACTIVE INGREDIENT SMD1X3XO9M TRIAZOLAM TABLET [PD-RX PHARMACEUTICALS, INC.] 3 silicon dioxide INACTIVE INGREDIENT ETJ7Z6XBU4 TRIAZOLAM TABLET [PD-RX PHARMACEUTICALS, INC.] 3 sodium benzoate INACTIVE INGREDIENT OJ245FE5EU TRIAZOLAM TABLET [PD-RX PHARMACEUTICALS, INC.] 3 starch, corn INACTIVE INGREDIENT O8232NY3SJ TRIAZOLAM TABLET [PD-RX PHARMACEUTICALS, INC.] 3
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 2 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 55289-787-60 55289078760 60 TABLET in 1 BOTTLE, PLASTIC (55289-787-60) 60 tablet 2010-10-18 0000-00-00 No No Current