bupropion
- Product NDC
- 68788-9255
- 11-digit product format
- 687889255
- Labeler code
- 68788
- Product ID
- 68788-9255_114736f0-0819-4541-b265-0461d873e90e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA201567
- Marketing category
- ANDA
- Marketing start
- 2014-11-03
- Marketing end
- 0000-00-00
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 300 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record