BUPROPION HYDROCHLORIDE (SR)
- Product NDC
- 58118-0878
- 11-digit product format
- 581180878
- Labeler code
- 58118
- Product ID
- 58118-0878_8d82a0de-c830-1afd-e053-2a95a90a6144
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale, LLC
- Application
- ANDA206674
- Marketing category
- ANDA
- Marketing start
- 2018-02-06
- Marketing end
- 2019-09-01
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record