Bupropion hydrochloride
- Product NDC
- 55154-4392
- 11-digit product format
- 551544392
- Labeler code
- 55154
- Product ID
- 55154-4392_3ebee532-691a-4a6e-8243-198087a4b94b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Cardinal Health, Inc.
- Application
- ANDA090325
- Marketing category
- ANDA
- Marketing start
- 2010-05-28
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record