FDA.reportPublic FDA data

Bupropion Hydrochloride

Product NDC
50090-0861
11-digit product format
500900861
Labeler code
50090
Product ID
50090-0861_fff22b87-496b-4858-936d-5d2253560fd5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
bupropion hydrochloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA079095
Marketing category
ANDA
Marketing start
2009-07-02
Marketing end
0000-00-00
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
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-0861-0EA - Each50090-0861d0219d1b-b605-4443-b93d-78b6b923c72f12018-10-11
50090-0861-1EA - Each50090-086117581409-5215-4854-a56a-cf11d8e508db12018-10-11
50090-0861-2EA - Each50090-08619ac5b8ec-2b05-4c9d-be1c-6255b78552b612018-10-11
50090-0861-3EA - Each50090-0861d856f572-f224-4e4f-9598-af7bdcddd20912018-10-11