| NDC Code | 69097-072-12 |
|---|
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-072-12) |
|---|
| Product NDC | 69097-072 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Bupropion Hydrochloride |
|---|
| Non-Proprietary Name | Bupropion Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20231025 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA207479 |
|---|
| Manufacturer | Cipla USA., Inc. |
|---|
| Substance Name | BUPROPION HYDROCHLORIDE |
|---|
| Strength | 300 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA] |
|---|