Forfivo

Product NDC
49909-010
11-digit product format
499090010
Labeler code
49909
Product ID
49909-010_dcb655a0-d646-4005-9c20-e58ef2be145e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
bupropion hydrochloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Edgemont Pharmaceuticals, LLC
Application
NDA022497
Marketing category
NDA
Marketing start
2012-10-01
Marketing end
2020-01-31
Substance
BUPROPION HYDROCHLORIDE
Active strength
450 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
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49909-010-30EA - Each49909-010a92596ee-a38c-4ea9-af2c-45caf0ca9c3e12013-02-13