| NDC Code | 55648-107-05 |
|---|
| Package Description | 10 BLISTER PACK in 1 CARTON (55648-107-05) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (55648-107-07) |
|---|
| Product NDC | 55648-107 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Bupropion Hydrochloride |
|---|
| Proprietary Name Suffix | (sr) |
|---|
| Non-Proprietary Name | Bupropion Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20120830 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA201331 |
|---|
| Manufacturer | Wockhardt Limited |
|---|
| Substance Name | BUPROPION HYDROCHLORIDE |
|---|
| Strength | 200 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA] |
|---|