Bupropion Hydrochloride - Bupropion Hydrochloride
Navigation: NDC > Supplier starting with: N > NORTHSTAR RX LLC| Field | Value |
|---|---|
| NDC Code: | 16714-336 |
| Proprietary Name: | Bupropion Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Bupropion Hydrochloride |
| Dosage Form: | TABLET, FILM COATED, EXTENDED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 01-05-2012 |
| Category Name: | ANDA |
| Application Number: | ANDA077455 |
| Labeler: | NORTHSTAR RX LLC |
| Substance Name: | BUPROPION HYDROCHLORIDE |
| Active Numerator Strength: | 200 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA] |
| DEA Schedule: |