FDA.reportPublic FDA data

Bupropion Hydrochloride

Product NDC
0904-7505
11-digit product format
009047505
Labeler code
0904
Product ID
0904-7505_a51e3361-63f9-4a1f-aa58-1619355f075b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Bupropion Hydrochloride
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Major Pharmaceuticals
Application
ANDA090693
Marketing category
ANDA
Marketing start
2024-11-25
Substance
BUPROPION HYDROCHLORIDE
Active strength
150 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

Additional Listing Data#

Finished product
Yes
Brand name base
Bupropion Hydrochloride
Brand name suffix
XL
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BUPROPION HYDROCHLORIDE150 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiZG7E5POY8O
Rxcui993541, 993557

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4eceb285-f3c7-4092-a21a-4c9f3169f20cProduct name520260220
548ba7fd-fd0c-4a21-b2b0-d01bf93143b8Product name320240209
43a1ed49-eae2-4840-8075-cb4b33478540Product name120230425
b8ee525f-67fb-39fb-91da-7e47ac54581dProduct name520200611
2e254488-9fcb-41b3-a7c3-e2c9a3941b29Product name120200603
b4ff0805-126a-406d-9cae-fc34fd8e8889Product name120190711
98e65af1-f5d0-75d5-c930-f8a4ce4c3284Product name920190211
e4d463bc-c674-43cb-be06-82786f310d01Product name120150326
0916dcfb-331f-89b1-8eac-6f7dc76d82daProduct name120140508
d7fc3d53-5a6c-de82-2808-1780f175f17eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0904-7505-04Bupropion HydrochlorideXL1 in 1 BLISTER PACKTABLET, EXTENDED RELEASE15
0904-7505-04Bupropion HydrochlorideXL30 in 1 CARTONTABLET, EXTENDED RELEASE305
0904-7505-61Bupropion HydrochlorideXL100 in 1 CARTONTABLET, EXTENDED RELEASE1005
0904-7505-61Bupropion HydrochlorideXL1 in 1 BLISTER PACKTABLET, EXTENDED RELEASE15

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0904-7505-04EA - Each0904-750505df23ed-b3da-40a1-a676-1fd28afafd8b12025-01-14
0904-7505-61EA - Each0904-7505f90a3fbc-9393-41f1-9acb-465cc305ef2512025-03-04

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0904-7505BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE [MAJOR PHARMACEUTICALS]2Current NDC, 4 package rows20241127_aa3d3e5b-74a3-47f6-b9aa-d6e248e950e5.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
993541buPROPion HCl 150 MG 24HR Extended Release Oral TabletPSNaa3d3e5b-74a3-47f6-b9aa-d6e248e950e55
993557buPROPion HCl 300 MG 24HR Extended Release Oral TabletPSNaa3d3e5b-74a3-47f6-b9aa-d6e248e950e55
99354124 HR bupropion hydrochloride 150 MG Extended Release Oral TabletSCDaa3d3e5b-74a3-47f6-b9aa-d6e248e950e55
99355724 HR bupropion hydrochloride 300 MG Extended Release Oral TabletSCDaa3d3e5b-74a3-47f6-b9aa-d6e248e950e55
993541bupropion HCl XL 150 MG 24 HR Extended Release Oral TabletSYaa3d3e5b-74a3-47f6-b9aa-d6e248e950e55
993557bupropion HCl XL 300 MG 24 HR Extended Release Oral TabletSYaa3d3e5b-74a3-47f6-b9aa-d6e248e950e55

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
0904-7505-040090475050430 BLISTER PACK in 1 CARTON (0904-7505-04) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK30 blister pack2024-11-25NoNoHistorical
0904-7505-6100904750561100 BLISTER PACK in 1 CARTON (0904-7505-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK100 blister pack2024-11-25NoNoHistorical