Bupropion Hydrochloride

Product NDC
60429-216
11-digit product format
604290216
Labeler code
60429
Product ID
60429-216_92b0ce28-148e-c739-e053-2995a90a98d2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
bupropion hydrochloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Golden State Medical Supply, Inc.
Application
ANDA079095
Marketing category
ANDA
Marketing start
2009-03-24
Marketing end
0000-00-00
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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60429-216-01EA - Each60429-21682d597d7-5ec0-4478-8ff0-ebf3192b65de12015-09-10
60429-216-05EA - Each60429-216ef2ffda0-7425-4158-9e3a-a0f9c836ae2f12020-01-03
60429-216-60EA - Each60429-216c640fcde-ef88-4f6b-8f6c-a481a0679c6312020-01-03