FDA.reportPublic FDA data

Bupropion Hydrochloride

Product NDC
68788-7807
11-digit product format
687887807
Labeler code
68788
Product ID
68788-7807_9dcdbb58-8617-4384-b60e-44483c1d63c2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
bupropion hydrochloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA205794
Marketing category
ANDA
Marketing start
2020-10-28
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
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Bupropion Hydrochloride
Brand name suffix
SR
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BUPROPION HYDROCHLORIDE150 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiZG7E5POY8O
Rxcui993518

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
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
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
68788-7807-1Bupropion HydrochlorideSR100 in 1 BOTTLE, PLASTICTABLET, FILM COATED, EXTENDED RE1008
68788-7807-2Bupropion HydrochlorideSR20 in 1 BOTTLE, PLASTICTABLET, FILM COATED, EXTENDED RE208
68788-7807-3Bupropion HydrochlorideSR30 in 1 BOTTLE, PLASTICTABLET, FILM COATED, EXTENDED RE308
68788-7807-6Bupropion HydrochlorideSR60 in 1 BOTTLE, PLASTICTABLET, FILM COATED, EXTENDED RE608
68788-7807-8Bupropion HydrochlorideSR120 in 1 BOTTLE, PLASTICTABLET, FILM COATED, EXTENDED RE1208
68788-7807-9Bupropion HydrochlorideSR90 in 1 BOTTLE, PLASTICTABLET, FILM COATED, EXTENDED RE908

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68788-7807BUPROPION HYDROCHLORIDE SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [PREFERRED PHARMACEUTICALS, INC.]7Current NDC, Legacy NDC, 6 package rows20250213_0b33fb1f-a7f0-4ab7-a882-eca2d2c77afa.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
993518buPROPion HCl 150 MG 12HR Extended Release Oral TabletPSN0b33fb1f-a7f0-4ab7-a882-eca2d2c77afa8
99351812 HR bupropion hydrochloride 150 MG Extended Release Oral TabletSCD0b33fb1f-a7f0-4ab7-a882-eca2d2c77afa8
993518bupropion HCl 150 MG 12 HR Extended Release Oral TabletSY0b33fb1f-a7f0-4ab7-a882-eca2d2c77afa8

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68788-7807-168788780701100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-1) 2020-10-280000-00-00NoNoCurrent
68788-7807-26878878070220 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-2) 2020-10-280000-00-00NoNoCurrent
68788-7807-36878878070330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-3) 2020-10-280000-00-00NoNoCurrent
68788-7807-66878878070660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-6) 2020-10-280000-00-00NoNoCurrent
68788-7807-868788780708120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-8) 2020-10-280000-00-00NoNoCurrent
68788-7807-96878878070990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-9) 2020-10-280000-00-00NoNoCurrent