Home NDC 82804-048 Amitriptyline Hydrochloride
Product NDC 82804-048
11-digit product format 828040048
Labeler code 82804
Product ID 82804-048_6dc9d113-1156-43ec-a7eb-253c2ff6bcfa
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Amitriptyline Hydrochloride
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Proficient Rx LP
Application ANDA214548
Marketing category ANDA
Marketing start 2021-05-26
Substance AMITRIPTYLINE HYDROCHLORIDE
Active strength 75 mg/1
Pharmacologic classes Tricyclic Antidepressant [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
Orange Book products# Current product rows page 1 of 1 · 6 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A214548-001 AMITRIPTYLINE HYDROCHLORIDE AMITRIPTYLINE HYDROCHLORIDE 10MG TABLET / ORAL AB 2021-05-19 A214548-002 AMITRIPTYLINE HYDROCHLORIDE AMITRIPTYLINE HYDROCHLORIDE 25MG TABLET / ORAL AB 2021-05-19 A214548-003 AMITRIPTYLINE HYDROCHLORIDE AMITRIPTYLINE HYDROCHLORIDE 50MG TABLET / ORAL AB 2021-05-19 A214548-004 AMITRIPTYLINE HYDROCHLORIDE AMITRIPTYLINE HYDROCHLORIDE 75MG TABLET / ORAL AB 2021-05-19 A214548-005 AMITRIPTYLINE HYDROCHLORIDE AMITRIPTYLINE HYDROCHLORIDE 100MG TABLET / ORAL AB 2021-05-19 A214548-006 AMITRIPTYLINE HYDROCHLORIDE AMITRIPTYLINE HYDROCHLORIDE 150MG TABLET / ORAL AB 2021-05-19
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 6 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 6 · 210 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 A214548-001 AMITRIPTYLINE HYDROCHLORIDE 10MG TABLET / ORAL AB 2021-05-19 84e616aacf4f…2026-09-14 22:38:34 2026-08 A214548-002 AMITRIPTYLINE HYDROCHLORIDE 25MG TABLET / ORAL AB 2021-05-19 84e616aacf4f…2026-09-14 22:38:34 2026-08 A214548-003 AMITRIPTYLINE HYDROCHLORIDE 50MG TABLET / ORAL AB 2021-05-19 84e616aacf4f…2026-09-14 22:38:34 2026-08 A214548-004 AMITRIPTYLINE HYDROCHLORIDE 75MG TABLET / ORAL AB 2021-05-19 84e616aacf4f…2026-09-14 22:38:34 2026-08 A214548-005 AMITRIPTYLINE HYDROCHLORIDE 100MG TABLET / ORAL AB 2021-05-19 84e616aacf4f…2026-09-14 22:38:34 2026-08 A214548-006 AMITRIPTYLINE HYDROCHLORIDE 150MG TABLET / ORAL AB 2021-05-19 84e616aacf4f…2026-08-18 06:07:40 2026-07 A214548-001 AMITRIPTYLINE HYDROCHLORIDE 10MG TABLET / ORAL AB 2021-05-19 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A214548-002 AMITRIPTYLINE HYDROCHLORIDE 25MG TABLET / ORAL AB 2021-05-19 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A214548-003 AMITRIPTYLINE HYDROCHLORIDE 50MG TABLET / ORAL AB 2021-05-19 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A214548-004 AMITRIPTYLINE HYDROCHLORIDE 75MG TABLET / ORAL AB 2021-05-19 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A214548-005 AMITRIPTYLINE HYDROCHLORIDE 100MG TABLET / ORAL AB 2021-05-19 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A214548-006 AMITRIPTYLINE HYDROCHLORIDE 150MG TABLET / ORAL AB 2021-05-19 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A214548-001 AMITRIPTYLINE HYDROCHLORIDE 10MG TABLET / ORAL AB 2021-05-19 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A214548-002 AMITRIPTYLINE HYDROCHLORIDE 25MG TABLET / ORAL AB 2021-05-19 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A214548-003 AMITRIPTYLINE HYDROCHLORIDE 50MG TABLET / ORAL AB 2021-05-19 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A214548-004 AMITRIPTYLINE HYDROCHLORIDE 75MG TABLET / ORAL AB 2021-05-19 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A214548-005 AMITRIPTYLINE HYDROCHLORIDE 100MG TABLET / ORAL AB 2021-05-19 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A214548-006 AMITRIPTYLINE HYDROCHLORIDE 150MG TABLET / ORAL AB 2021-05-19 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A214548-001 AMITRIPTYLINE HYDROCHLORIDE 10MG TABLET / ORAL AB 2021-05-19 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A214548-002 AMITRIPTYLINE HYDROCHLORIDE 25MG TABLET / ORAL AB 2021-05-19 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A214548-003 AMITRIPTYLINE HYDROCHLORIDE 50MG TABLET / ORAL AB 2021-05-19 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A214548-004 AMITRIPTYLINE HYDROCHLORIDE 75MG TABLET / ORAL AB 2021-05-19 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A214548-005 AMITRIPTYLINE HYDROCHLORIDE 100MG TABLET / ORAL AB 2021-05-19 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A214548-006 AMITRIPTYLINE HYDROCHLORIDE 150MG TABLET / ORAL AB 2021-05-19 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A214548-001 AMITRIPTYLINE HYDROCHLORIDE 10MG TABLET / ORAL AB 2021-05-19 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A214548-002 AMITRIPTYLINE HYDROCHLORIDE 25MG TABLET / ORAL AB 2021-05-19 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A214548-003 AMITRIPTYLINE HYDROCHLORIDE 50MG TABLET / ORAL AB 2021-05-19 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A214548-004 AMITRIPTYLINE HYDROCHLORIDE 75MG TABLET / ORAL AB 2021-05-19 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A214548-005 AMITRIPTYLINE HYDROCHLORIDE 100MG TABLET / ORAL AB 2021-05-19 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A214548-006 AMITRIPTYLINE HYDROCHLORIDE 150MG TABLET / ORAL AB 2021-05-19 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A214548-001 AMITRIPTYLINE HYDROCHLORIDE 10MG TABLET / ORAL AB 2021-05-19 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A214548-002 AMITRIPTYLINE HYDROCHLORIDE 25MG TABLET / ORAL AB 2021-05-19 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A214548-003 AMITRIPTYLINE HYDROCHLORIDE 50MG TABLET / ORAL AB 2021-05-19 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A214548-004 AMITRIPTYLINE HYDROCHLORIDE 75MG TABLET / ORAL AB 2021-05-19 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A214548-005 AMITRIPTYLINE HYDROCHLORIDE 100MG TABLET / ORAL AB 2021-05-19 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A214548-006 AMITRIPTYLINE HYDROCHLORIDE 150MG TABLET / ORAL AB 2021-05-19 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A214548-001 AMITRIPTYLINE HYDROCHLORIDE 10MG TABLET / ORAL AB 2021-05-19 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A214548-002 AMITRIPTYLINE HYDROCHLORIDE 25MG TABLET / ORAL AB 2021-05-19 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A214548-003 AMITRIPTYLINE HYDROCHLORIDE 50MG TABLET / ORAL AB 2021-05-19 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A214548-004 AMITRIPTYLINE HYDROCHLORIDE 75MG TABLET / ORAL AB 2021-05-19 b8a1b40f171c…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 6 · 210 observed states.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Amitriptyline Hydrochloride
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AMITRIPTYLINE HYDROCHLORIDE 75 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 26LUD4JO9K Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 856853 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 82804-048-30 Amitriptyline Hydrochloride 30 in 1 BOTTLE TABLET, FILM COATED 30 1 82804-048-60 Amitriptyline Hydrochloride 60 in 1 BOTTLE TABLET, FILM COATED 60 1 82804-048-90 Amitriptyline Hydrochloride 90 in 1 BOTTLE TABLET, FILM COATED 90 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82804-048 AMITRIPTYLINE HYDROCHLORIDE TABLET, FILM COATED [PROFICIENT RX LP] 1 Current NDC, 3 package rows 20231223_6dc9d113-1156-43ec-a7eb-253c2ff6bcfa.zip
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 3 of 3 · 44 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Amitriptyline Hydrochloride AMITRIPTYLINE HYDROCHLORIDE Proficient Rx LP 6dc9d113-1156-43ec-a7eb-253c2ff6bcfa 2023-12-01 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 214548 application number: ANDA214548 ndc (product): 82804-048 Amitriptyline Hydrochloride AMITRIPTYLINE HYDROCHLORIDE Proficient Rx LP e42225f5-44bd-451e-98a1-aa3877457733 2023-08-04 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 214548 application number: ANDA214548 Amitriptyline Hydrochloride AMITRIPTYLINE HYDROCHLORIDE A-S Medication Solutions 1a622039-0a79-407c-8f15-2ea0c5844136 2023-04-07 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 214548 application number: ANDA214548 Amitriptyline Hydrochloride AMITRIPTYLINE HYDROCHLORIDE Aphena Pharma Solutions - Tennessee, LLC 8746c047-51b9-4040-aeec-cd1f5b6eb3d4 2023-03-20 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 214548 application number: ANDA214548
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 82804-048-30 82804004830 30 TABLET, FILM COATED in 1 BOTTLE (82804-048-30) 2023-12-21 No No Current 82804-048-60 82804004860 60 TABLET, FILM COATED in 1 BOTTLE (82804-048-60) 2023-12-21 No No Current 82804-048-90 82804004890 90 TABLET, FILM COATED in 1 BOTTLE (82804-048-90) 2023-12-21 No No Current