Budeprion

Product NDC
63629-3762
11-digit product format
636293762
Labeler code
63629
Product ID
63629-3762_45fa1a0a-5ee3-4cc2-b2cc-d7c12bed54a2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Bupropion Hydrochloride
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA077284
Marketing category
ANDA
Marketing start
2008-05-30
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
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-3762-1EA - Each63629-376247f6ebf0-5722-416e-90b2-1efd7b1f7be512015-10-02
63629-3762-2EA - Each63629-37623276598d-7572-4167-8ba7-d94fcdf2a14f12015-10-02
63629-3762-3EA - Each63629-37625dd471e6-7722-44fd-bb4a-44e7128112a712017-03-06
63629-3762-4EA - Each63629-3762e868f92e-897a-4d30-8bb3-3b4bcf6b743b12017-03-06