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