Home NDC 72189-457 Bupropion HCL
Product NDC 72189-457
11-digit product format 721890457
Labeler code 72189
Product ID 72189-457_2c4dd247-ae5a-fe93-e063-6394a90a937c
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Bupropion HCL
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Direct_Rx
Application ANDA076143
Marketing category ANDA
Marketing start 2023-03-30
Substance BUPROPION HYDROCHLORIDE
Active strength 100 mg/1
Pharmacologic classes Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 72189-457-30 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 72189-457-30 0efc9e666f02…f202fb6c5f17…
Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
Orange Book products# Current product rows page 1 of 1 · 2 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A076143-001 BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 A076143-002 BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17
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 3 · 86 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 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 84e616aacf4f…2026-09-14 22:38:34 2026-08 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 84e616aacf4f…2026-08-18 06:07:40 2026-07 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 301d65b070ca…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 1e350fbaab3a…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 8072bd15b7f6…2024-05-31 18:47 UTC 2024-05 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 8072bd15b7f6…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 5c6f7cd8ea54…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 5c6f7cd8ea54…2022-04-08 23:34 UTC 2022-04 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 5d02ea3f76ae…2022-04-08 23:34 UTC 2022-04 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 5d02ea3f76ae…2022-04-04 05:41 UTC 2022-04 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 4b0b4de00fa7…2022-04-04 05:41 UTC 2022-04 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 4b0b4de00fa7…2019-12-13 00:20 UTC 2019-12 A076143-001 BUPROPION HYDROCHLORIDE 75MG TABLET / ORAL AB 2006-01-17 74a2ff9319b5…2019-12-13 00:20 UTC 2019-12 A076143-002 BUPROPION HYDROCHLORIDE 100MG TABLET / ORAL AB RS 2006-01-17 74a2ff9319b5…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 3 · 86 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 Bupropion HCL
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BUPROPION HYDROCHLORIDE 100 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination ZG7E5POY8O Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 993687 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 72189-457-30 Bupropion HCL 30 in 1 BOTTLE TABLET, FILM COATED 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72189-457 BUPROPION HCL TABLET, FILM COATED [DIRECT_RX] 2 Current NDC, 1 package rows 20250123_f820ad7d-3c88-4a4f-e053-6294a90aef7b.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 2 of 2 · 25 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Bupropion Hydrochloride BUPROPION HYDROCHLORIDE Proficient Rx LP 13560bf8-eb25-44f0-968e-db70d51219af 2024-07-01 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 076143 application number: ANDA076143 Bupropion Hydrochloride BUPROPION HYDROCHLORIDE A-S Medication Solutions 78ef709a-f835-4b03-92dd-16a4c82af0c1 2024-05-31 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 076143 application number: ANDA076143 Bupropion Hydrochloride BUPROPION HYDROCHLORIDE Aphena Pharma Solutions - Tennessee, LLC 8d80f882-1887-4d73-b09f-e98fd7ef2acb 2024-02-06 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 076143 application number: ANDA076143 Bupropion Hydrochloride BUPROPION HYDROCHLORIDE Aphena Pharma Solutions - Tennessee, LLC b0e10a21-0ae3-4a8b-bd3e-7a48b30f8418 2023-05-16 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 076143 application number: ANDA076143 Bupropion Hydrochloride BUPROPION HYDROCHLORIDE Aphena Pharma Solutions - Tennessee, LLC 7d81ed30-ddf7-431a-84f8-6c630cf2b977 2018-10-18 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 076143 application number: ANDA076143
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 72189-457-30 72189045730 30 TABLET, FILM COATED in 1 BOTTLE (72189-457-30) 2023-03-30 No No Current