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Bupropion hydrochloride
Bupropion hydrochloride - 47335-738-08 - (Bupropion hydrochloride)
Drug Information of Bupropion hydrochloride
| Product NDC: | 47335-738 |
| Proprietary Name: | Bupropion hydrochloride |
| Non Proprietary Name: | Bupropion hydrochloride |
| Active Ingredient(s): | 200 mg/1 & nbsp; Bupropion hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bupropion hydrochloride
| Product NDC: | 47335-738 |
| Labeler Name: | Sun Pharma Global FZE |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078866 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100408 |
Package Information of Bupropion hydrochloride
| Package NDC: | 47335-738-08 |
| Package Description: | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-08) |
NDC Information of Bupropion hydrochloride
| NDC Code | 47335-738-08 |
| Proprietary Name | Bupropion hydrochloride |
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-08) |
| Product NDC | 47335-738 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Bupropion hydrochloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100408 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global FZE |
| Substance Name | BUPROPION HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA] |
